Harry E. Claiborne, a judge on the U.S. District Court for the District of Nevada, was impeached and removed from office on charges of income tax evasion in 1986. It was the first time that a judge had been impeached in more than five decades.

Impeachment Proceedings for Harry Claiborne
In 1984, Judge Claiborne became the first sitting Federal judge in the U.S. history to be found guilty of a felony when he was convicted of filing false income tax returns.

Prosecutors alleged that the federal judge failed to pay taxes on $106,000 in income he received in 1979 and 1980 for legal services performed prior to becoming a judge. Claiborne ultimately served 17 months of a two-year sentence before his release in 1987.

Judge Claiborne maintained his innocence, arguing that the charges were the result of a vendetta by federal prosecutors whom he ruled against in his courtroom. When Claiborne refused to resign after his conviction, the U.S. House of Representative began impeachment proceedings. Claiborne was subsequently impeached by the U.S. House of Representatives by a 406-to-0 vote. The four articles of impeachment included charges of tax evasion and bringing “disrepute” on the Federal court system.

Instead of the full Senate serving as a High Court of Impeachment, the Senate established a 12-member panel to conduct the trial. Relying on a never-before-used Senate rule adopted in 1935, the committee examined the evidence, heard testimony, and presented its findings to the full Senate. During closing arguments, Claiborne’s counsel unsuccessfully argued that the use of a trial committee was unconstitutional. The full Senate voted convict Claiborne, marking the first time the Senate tried and convicted a federal official who had already been convicted in a criminal court. Claiborne was removed from office on October 9, 1986.
For a full list of all Federal Judges that have been impeached please visit our Impeachment of Federal Judges page.

resource: constitutionallawreport.com

Impeachment of Andrew Johnson

Fact 1: President Abraham Lincoln was assassinated in April 1865 and Vice President Andrew Johnson assumed the role of President of the United States at the end of the Civil War, as the Reconstruction of the South was just beginning
 Fact 2: Andrew Johnson was a Southern Democrat and, as such, had sympathies with the Confederacy and granted pardons to ex-Confederates on a large scale. He was inexperienced, a stubborn man with little patience. The government consisted of many radical Republicans and before long the President and Congress were in conflict due to Reconstruction Policies.
Fact 3: The radical Republicans believed that the President was behaving too leniently towards the Southern states who were attempting to restore self-rule and passing state laws referred to as the Black Codes. At the end of 1865, just six months after the end of the Civil War Andrew Johnson declared the end of Reconstruction.

Fact 4: The radical Republicans were outraged and were determined to establish a Congressional Reconstruction. The Southern Democrat President and the radical Republicans were in direct conflict and on a collision course that would end with the Impeachment of the President.
Fact 5: The President further infuriated Congress by vetoing an extension to the Freedmen’s Bureau
Fact 6: Republicans passed the Civil Rights Act of 1866 overriding the President’s veto.
Fact 7: The radicals become more powerful by gaining a two-thirds margin in the 1866 Congressional elections
Fact 8: Congress develop plans for the reunification of the South which will be referred to as Congressional Reconstruction
Fact 9: Congress passed the first of the Reconstruction Acts, overriding the President’s veto, which gave them military and political control of the Southern states.
Fact 10: The President replaces several generals who command the 5 military districts established by the Reconstruction Acts

Fact 11: Congress passed the Tenure of Office Act on March 2, 1867, overriding the President’s veto, to limit the President’s powers and prevent him dismissing radical Republicans from office.
Fact 12: The Tenure of Office Act was also passed to stop the President interfering with the Congressional plans for Reconstruction
Fact 13: The Tenure of Office Act forbids the President to remove any federal office-holder appointed by at the Senate without the further approval of the Senate
Fact 14: The Tenure of Office Act also provides that the President’s cabinet should hold office for the full term of the President plus one month, subject to removal by the Senate
Fact 15: The President is furious regarding the Tenure of Office Act claiming it is unconstitutional
Fact 16: The President continues to oppose congressional policy, and insists on the removal of the radical Secretary of War, Edwin M. Stanton, in defiance of the Tenure of Office Act .
Fact 17: Edwin Stanton, as Secretary of War, was an important member of the cabinet and a firm supporter of the radical Republicans
 Fact 18: Edwin Stanton was in open opposition to the policies of the President
Fact 19: Edwin Stanton refused to move and barricaded himself in his office claiming that the Tenure of Office Act protected him.
Fact 20: Congress supported Edwin Stanton’s claims asserting that by suspending Edwin Stanton and removing him from his cabinet without the consent of Congress, the President Johnson had breached the Tenure of Office Act.
Fact 21: Congress started Impeachment Proceedings against the President

Fact 22: Impeachment is a criminal proceeding against a public official requiring formal documentation and Articles of impeachment
Fact 23: It is the right of the House of Representatives to impeach. It is the right of the Senate to try and determine impeachments.
Fact 24: Constitution: The Constitution of the United States refers to the process of Impeachment in Article II, Section 4 of the Constitution.
Fact 25: On Monday, February 24, 1868, the House of Representatives resolved to impeach Andrew Johnson of high crimes and misdemeanors
Fact 26: On Monday the March 2, 1868, eleven articles of impeachment were agreed by the House of Representatives.
Fact 27: On March 2, 1868 the Articles of Impeachment were presented to the Senate and the grand inquest of the nation is set to begin

Fact 28: March 30, 1868: The impeachment trial of Johnson begins in the Senate

Fact 29: May 16, 1868: The Senate voted on the 11th Article of Impeachment and is one vote short of the 2/3 majority needed to impeach the President

 Fact 30: May 26, 1868: The final vote was taken in the Senate on the second and third Articles of Impeachment and Johnson was again acquitted. The Impeachment trial of Andrew Johnson is over.

american-historama.org

• North Bay Produce, Inc. of Traverse City, Michigan is voluntarily recalling 2,297 cases and 2 bulk bins of fresh apples due to the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  Recalled varieties include McIntosh, Honeycrisp, Jonathan, Fuji, Jonamac and Red Delicious apples. Recalled apples were sold in plastic bags under the brands; Great Lakes, North Bay Produce Pure Michigan as well as unbranded in clear plastic tote bags, white paper tote bags, and individually from retailers display trays. The recalled apples were shipped between October 16th, 2019 and October 21st, 2019 from one North Bay facility to wholesalers, retailers and brokers in Florida, Illinois, Kentucky, Louisiana, Michigan, North Carolina, Texas and Wisconsin.
  Apples purchased at retail prior to October 16th are not affected by this recall, and no other North Bay Produce products are affected by this recall. At this time, we are not aware of any illnesses linked by health officials to this recall.
  Consumers can identify the recalled product by the following product descriptions and photos below:
  < <
  Distributed By
  Variety, Brand & Packaging
  Arrival Date(s)
  UPC Code
  PLU
  Number
  Item
  Number
  Shipped-To- Location
  North Bay
  Produce, Inc.
  McIntosh Great
  Lakes 3lb. Plastic
  Bag, Product of MIUSA
  Delivered between 10/19/19 and 10/21/19
  8 13635
  01012 8Michigan Louisiana
  North Bay
  Produce, Inc.
  Jonathan
  Great Lakes 3lb. Plastic Bag, Product of MI-USA
  Delivered 10/21/19
  8 13635
  01017 3Louisiana
  North Bay
  Produce, Inc.
  Honeycrisp Great
  Lakes 3lb. Plastic
  Bag, Product of MI-
  Delivered 10/21/19
  8 13635
  01018 0

  Louisiana

  USA

  North Bay
  Produce, Inc.
  Jonamac Great
  Lakes 3lb. Plastic
  Bag, Product of MIUSA
  Delivered 10/16/19
  8 13635
  01019 7

  Wisconsin
  North Bay
  Produce, Inc.
  McIntosh North Bay Pure Michigan 3lb. Plastic Bag, Product of MI-USA
  Delivered 10/21/19
  8 13635
  01012 8

  Michigan
  North Bay
  Produce, Inc.
  Honeycrisp North
  Bay Pure Michigan
  2lb. Plastic Bag,
  Product of MI-USA
  Delivered 10/19/19
  8 13635
  01130 9

  Michigan
  North Bay
  Produce, Inc.
  Honeycrisp Quarter
  Peck Paper Tote
  Bag, Product of MIUSA
  Delivered 10/19/19

  700116
  Michigan
  North Bay
  Produce, Inc.
  Fuji
  Half Peck Plastic Tote Bags, Product of MI-USA
  Delivered 10/18/19

  4195

  All Fresh Thyme
  Farmers Market
  Stores
  North Bay
  Produce, Inc.
  Jonathan Bulk 600lb
  Corugated Bins,
  Product of MI-USA
  Delivered 10/16/19

  Michigan

  North Bay
  Produce, Inc.
  Mcintosh
  Distributed in trays;
  Product of MI-USA
  Delivered
  10/19/19 &
  10/21/19

  4019

  Not sold at retail
  North Bay
  Produce, Inc.
  Red Delicious Distributed in trays; sold individually for retail sale, Product of MI-USA
  Delivered 10/21/19

  4168
  4167

  North Carolina
  Department of
  Agriculture (Food
  Distribution
  Division- Butner)
  Creedmoor, North Carolina
  Feeding South
  Florida
  Pembroke Park,
  Florida
  Anyone who has the recalled product in their possession should not consume it. The product should be discarded or returned to the place of purchase.
  The recall was initiated as a result of a finished product test that indicated the presence of the organism. Upon notification, we immediately ceased the production and distribution product from the identified facility and continue our investigation as to what caused the issue, in cooperation with FDA.
  We have notified our commercial customers to whom we shipped the recalled product and are working with them to remove recalled product from commerce.
  Consumers with questions may call 1-231-929-4001, Monday-Friday, 8am – 5pm Eastern Time, or visit http://www.northbayproduce.com
  External Link Disclaimer
  .

• King Arthur Flour, Inc. was notified by ADM Milling Co. that three additional product lot codes of Unbleached All-Purpose Flour 5 lb. were omitted from the original data they provided for the press release on October 3, 2019. The additional lot codes and their corresponding “Best Used By” dates are listed below:
  Best Used by Date 12/09/19: Lot codes L18A09A & L18A09C
  Best Used by Date 01/08/20: Lot code A19A08A
  This new information only applies to “Best Used By” dates already disclosed in the prior release. No additional Best Used By dates are introduced as a result of these three updated lot codes.
  As stated in the prior release, we have undertaken this voluntary recall because of the potential presence of E. coli 026.
  King Arthur Flour has not received any confirmed reports of illnesses to date related to this product.
  Consumers who have any of these affected products should throw them away and may submit a claim for a refund or replacement at kingarthurflour.com/voluntaryrecall
  External Link Disclaimer
  , or by calling our King Arthur Flour Consumer Hotline at 866-797-9178.
  Consumer safety is our top priority. Consumers are reminded to wash their hands, work surfaces, and utensils thoroughly after contact with raw dough products or flour, and to never eat raw dough or batter. The Centers for Disease Control (CDC) warns consumers to not consume raw products made with flour. E. coli O26 is killed by heat through baking, frying, sautéing, or boiling products made with flour. For more information, refer to the following: https://www.cdc.gov/features/no-raw-dough/index.html.
  Bakers have trusted King Arthur Flour products in their kitchens for over 225 years. We remain committed to providing our consumers safe and superior products.
  This information can be found online at kingarthurflour.com/voluntaryrecall.
  External Link Disclaimer
  Consumers with any questions regarding this recall or King Arthur Flour products are encouraged to call the King Arthur Flour Consumer Hotline at 866-797-9178.
  Original Press Release
• Mylan Pharmaceuticals Inc. is conducting a voluntary nationwide recall of one lot (see table below) of Alprazolam Tablets, USP C-IV 0.5 mg, to the consumer/user level. This lot is being recalled due to the potential presence of foreign substance. Clinical impact from the foreign material, if present, is expected to be rare, but the remote risk of infection to a patient cannot be ruled out. To date, Mylan has not received any adverse events related to this batch.
  Alprazolam Tablets are indicated for the management of anxiety disorder, the short-term relief of symptoms of anxiety, and the treatment of panic disorder, with or without agoraphobia.
  Alprazolam Tablets, USP C-IV 0.5 mg, are packaged in bottles of 500. This batch was distributed in the U.S. between July 2019 and August 2019. The recalled lot is as follows:
  NDC
  Product Description and Strength
  Size
  Lot number
  Expiry
  0378-4003-05
  Alprazolam Tablets, USP C-IV 0.5 mg
  Bottles of 500
  8082708
  September 2020
  Mylan has notified its distributors and customers by letter and is arranging for return of all recalled products. Following are actions for wholesalers, retailers and consumers:
  Wholesaler: Immediately examine your inventory, quarantine and discontinue distribution of these lots. In addition, if you have further distributed the product, please identify your retail level customers and provide a list of customers via Microsoft excel file to mylan5924@stericycle.com within 10 business days. Stericycle will notify your retail level customers that received the affected batches.
  Retailer: Immediately examine your inventory, quarantine and discontinue distribution of these lots. Additionally, if you have further distributed the product, please identify the consumer and notify them immediately of this product recall. The consumer should be instructed to contact Stericycle at 1-888-843-0255 for the documentation packet to return the product.
  Consumer: Please contact Stericycle at 1-888-843-0255 for the documentation packet to return product to Stericycle.
  Consumers with questions regarding this recall can contact Mylan Customer Relations at 800.796.9526 or customer.service@mylan.com, Monday through Friday from 8 a.m. – 5 p.m. EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
  Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
  Complete and submit the report Online
  Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
• North Bay Produce, Inc. of Traverse City, Michigan is voluntarily recalling 2,297 cases and 2 bulk bins of fresh apples due to the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  Recalled varieties include McIntosh, Honeycrisp, Jonathan, Fuji, Jonamac and Red Delicious apples. Recalled apples were sold in plastic bags under the brands; Great Lakes, North Bay Produce Pure Michigan as well as unbranded in clear plastic tote bags, white paper tote bags, and individually from retailers display trays. The recalled apples were shipped between October 16th, 2019 and October 21st, 2019 from one North Bay facility to wholesalers, retailers and brokers in Florida, Illinois, Kentucky, Louisiana, Michigan, North Carolina, Texas and Wisconsin.
  Apples purchased at retail prior to October 16th are not affected by this recall, and no other North Bay Produce products are affected by this recall. At this time, we are not aware of any illnesses linked by health officials to this recall.
  Consumers can identify the recalled product by the following product descriptions and photos below:
  < <
  Distributed By
  Variety, Brand & Packaging
  Arrival Date(s)
  UPC Code
  PLU
  Number
  Item
  Number
  Shipped-To- Location
  North Bay
  Produce, Inc.
  McIntosh Great
  Lakes 3lb. Plastic
  Bag, Product of MIUSA
  Delivered between 10/19/19 and 10/21/19
  8 13635
  01012 8Michigan Louisiana
  North Bay
  Produce, Inc.
  Jonathan
  Great Lakes 3lb. Plastic Bag, Product of MI-USA
  Delivered 10/21/19
  8 13635
  01017 3Louisiana
  North Bay
  Produce, Inc.
  Honeycrisp Great
  Lakes 3lb. Plastic
  Bag, Product of MI-
  Delivered 10/21/19
  8 13635
  01018 0LouisianaUSANorth Bay
  Produce, Inc.
  Jonamac Great
  Lakes 3lb. Plastic
  Bag, Product of MIUSA
  Delivered 10/16/19
  8 13635
  01019 7

  Wisconsin
  North Bay
  Produce, Inc.
  McIntosh North Bay Pure Michigan 3lb. Plastic Bag, Product of MI-USA
  Delivered 10/21/19
  8 13635
  01012 8

  Michigan
  North Bay
  Produce, Inc.
  Honeycrisp North
  Bay Pure Michigan
  2lb. Plastic Bag,
  Product of MI-USA
  Delivered 10/19/19
  8 13635
  01130 9

  Michigan
  North Bay
  Produce, Inc.
  Honeycrisp Quarter
  Peck Paper Tote
  Bag, Product of MIUSA
  Delivered 10/19/19

  700116
  Michigan
  North Bay
  Produce, Inc.
  Fuji
  Half Peck Plastic Tote Bags, Product of MI-USA
  Delivered 10/18/19

  4195

  All Fresh Thyme
  Farmers Market
  Stores
  North Bay
  Produce, Inc.
  Jonathan Bulk 600lb
  Corugated Bins,
  Product of MI-USA
  Delivered 10/16/19

  Michigan

  North Bay
  Produce, Inc.
  Mcintosh
  Distributed in trays;
  Product of MI-USA
  Delivered
  10/19/19 &
  10/21/19

  4019

  Not sold at retail
  North Bay
  Produce, Inc.
  Red Delicious Distributed in trays; sold individually for retail sale, Product of MI-USA
  Delivered 10/21/19

  4168
  4167

  North Carolina
  Department of
  Agriculture (Food
  Distribution
  Division- Butner)
  Creedmoor, North Carolina
  Feeding South
  Florida
  Pembroke Park,
  Florida
  Anyone who has the recalled product in their possession should not consume it. The product should be discarded or returned to the place of purchase.
  The recall was initiated as a result of a finished product test that indicated the presence of the organism. Upon notification, we immediately ceased the production and distribution product from the identified facility and continue our investigation as to what caused the issue, in cooperation with FDA.
  We have notified our commercial customers to whom we shipped the recalled product and are working with them to remove recalled product from commerce.
  Consumers with questions may call 1-231-929-4001, Monday-Friday, 8am – 5pm Eastern

• Ranitidine Syrup, 15 mg/mL (Ranitidine Oral Solution USP) by Lannett: Recall – Due to Levels of N-Nitrosodimethylamine (NDMA) above the Levels Recently Established by the FDAAUDIENCE: Patient, Consumer, Health Professional, PharmacyISSUE: Lannett Company is voluntarily recalling all lots within expiry of Ranitidine Syrup, 15mg/mL (Ranitidine Oral Solution USP) due to levels of NDMA above the levels recently established by the FDA for Ranitidine Hydrochloride Syrup (Ranitidine Oral Solution, USP). NDMA is classified as a probable human carcinogen, a substance that can cause cancer, based on laboratory testing. Lannett was notified by FDA of the potential presence of NDMA on September 17, 2019 and immediately commenced testing of the Active Pharmaceutical Ingredient (API) and drug product. The analysis confirmed the presence of NDMA.Please click the “Read Recall” button below to view the list of affected lots.RECOMMENDATION: Patients and consumers should contact their physician or health care provider if they have experienced any problems that may be related to taking or using this drug product.Patients, consumers and health care professionals are encouraged to report adverse events or side effects related to the use of these
• Update   George’s Prepared Foods, a Caryville, Tenn. establishment, is recalling approximately 6,444 pounds of ready-to-eat (RTE) pork sausage patty and turkey sausage patty products that may be contaminated with Salmonella, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The ready-to-eat pork and turkey sausage patty items were produced on April 19, 2019, April 27, 2019, May 7, 2019 and May 9, 2019. The following products are subject to recall: [View Labels (PDF only)]
  24.92-oz. packages containing “Great Value Fully Cooked Original Pork Sausage Patties” with use by date of 10/16/19 and lot code 1091971894.
  24.92-oz. packages containing “Great Value Fully Cooked Original Breakfast Turkey Patties” with use by date of 10/24/19 and lot code 1171971897.
  35.6-oz. packages containing “Family Size Great Value Fully Cooked Original Pork Sausage Patties” with use by date of 11/03/19 and lot code 1271972894 or use by date 11/05/19 and lot code 1291972894.
  The products subject to recall bear establishment number “EST. M2260T or P-2260T” printed on the package. These items were shipped to retail locations nationwide.
  The problem was discovered when the firm notified FSIS that the firm’s third-party cold storage facility had inadvertently shipped the ready-to-eat products to commerce.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  Consumption of ready-to-eat food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 12 to 72 hours after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop a severe illness. Individuals concerned about an illness should contact their health care provider.
  FSIS is concerned that some product may be frozen and in consumers’ refrigerators or freezers or both. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Media and consumers with questions regarding the recall can contact George’s Prepared Foods’ Customer Care Line at (800) 471-9665.
• ICU Medical, Inc. (Nasdaq: ICUI) is voluntarily recalling one single lot of Lactated Ringer’s Injection, USP, and one single lot of 0.9% Sodium Chloride Injection, USP. The products are being recalled to the hospital level due to the presence of particulate matter.
  Administration of a drug product that contains particulate matter could result in adverse events ranging from inflammation at the site of injection to more serious events that could include the formation of a blood clot obstructing the flow of blood which could lead to end-organ damage or death. To date, ICU Medical, Inc. has not received reports of adverse events related to this recall.
  The Lactated Ringer’s Injection, USP and 0.9% Sodium Chloride Injection are indicated for parenteral replacement of extracellular losses of fluid and electrolytes, with or without minimal carbohydrate calories, as required by the clinical condition of the patient. Intravenous solutions containing sodium chloride are indicated for parenteral replenishment of fluid and sodium chloride as required by the clinical condition of the patient. Product was distributed nationwide both by ICU Medical direct to customers and through medical distributors.
  The affected product lots, manufactured in the U.S. for ICU Medical by Hospira, a Pfizer company in late 2017 and early 2018, are listed below:
  NDC Number
  Product Description
  Lot Number*
  Expiration Date
  Configuration
  Manufacture
  Date
  Distribution
  Dates
  0409-7953-
  03
  Lactated Ringer’s
  Injection, USP
  84-603-FW
  01-Dec-2019
  500 mL Flexible
  Container
  December
  2017
  February 2018 –
  June 2018
  0409-7983-
  25
  0.9% Sodium
  Chloride Injection,
  USP
  95-101-C6
  01-May-2020
  250 mL VisIVTM
  Container
  November
  2018
  December 2018
  – March 2019
  ICU Medical is notifying its distributors and customers of this recall by letter and is arranging for the return of all recalled products. Hospitals/distributors that have product that is being recalled should stop use/further distribution and return to place of purchase.
  Customers with questions regarding this recall can call ICU Medical at 1-844-6547780 Monday through Friday between the hours of 8 a.m. and 5 p.m. Central time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these drug products.
  Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
  Complete and submit the report Online
  Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
  This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
• Wawona Frozen Foods is voluntarily recalling packages of frozen raspberries and frozen berry mixes containing raspberries sold at Aldi Grocery Stores and frozen raspberries sold at Raley’s Family of Fine Stores because they have the potential to be contaminated with Hepatitis A. The frozen raspberries and frozen berry mixes containing raspberries were packaged under the Aldi and Raley’s private labels. Wawona Frozen Foods is issuing this voluntary recall out of an abundance of caution due to a positive test result taken as part of a government sampling program.
  There have been no illnesses associated with this voluntary and precautionary recall to date.
  Hepatitis A is a contagious virus that can cause liver disease. A Hepatitis A virus (HAV) infection can range in severity from a mild illness lasting a few weeks to a severe illness lasting several months. In rare cases, particularly consumers who have a pre-existing severe illness or are immune compromised, Hepatitis A infections can progress to liver failure. Illness usually occurs within 15 to 50 days after eating or drinking contaminated food or water. Symptoms of Hepatitis A infection include fever, headache, fatigue, loss of appetite, nausea, vomiting, diarrhea, abdominal pain, jaundice, dark urine or pale stool. In some instances, particularly in children under the age of six, Hepatitis A infection may be asymptomatic. Persons who may have consumed affected product should consult their health care provider or local health department to determine if a vaccination is appropriate and consumers with symptoms of Hepatitis A should contact their health providers or the local health department immediately.
  The recalled frozen raspberries were packaged and sold in these sizes and with the following accompanying information:
  Aldi:
  Season’s Choice Raspberries (frozen): 12 ounce bags, “best by” date of June, 10, 2021, August 1,2021 and August 23, 2021. “Product of Chile.” UPC Code: 0 41498 12419 9 o Season’s Choice Berry Medley (frozen) containing raspberries: 16 ounce bags, “best by” date of July 17, 2021, July 20, 2021 and July 22, 2021. “Product of USA, Chile.” UPC Code: 0 41498 31344 9 Raley’s:
  Raley’s Fresh Frozen Red Raspberries: 12 ounce bags, “best by” date of June 5, 2021 (lot code:20156A04), August 1, 2021 (lot code: 20213A06) “Product of Chile.” UPC Code: 46567 00754
  The frozen raspberries and frozen berry mixes containing raspberries were distributed throughout stores in Aldi and Raley’s Family of Fine store chains. The recalled frozen raspberries were imported from Chile. No other retail packages of frozen raspberry products are included in this voluntary and precautionary recall.
  Consumers who have purchased the above products should not consume them and should either discard them or return them to the place of purchase for a full refund. Aldi and Raley customers with questions may contact Wawona Frozen Foods at 866-913-0667 or visit the website at http://www.wawona.com.
  Wawona Frozen Foods is fully cooperating with federal health officials as well as Aldi and Raley’s to facilitate an efficient and complete recall of the frozen raspberries and frozen berry mixes containing raspberries.
  “Wawona is a third-generation family company that emphasizes a culture of accountability, commitment and integrity. This voluntary recall is a reflection of that culture and our commitment to ensuring the safety of our consumers, says Bill Smittcamp, President of Wawona Frozen Foods.”

• Nestlé USA is initiating a voluntary recall of ready-to-bake refrigerated Nestlé Toll House Cookie Dough products due to the potential presence of food-grade rubber pieces. This voluntary recall only covers specific batch codes of the following products, which include ready-to-bake refrigerated Nestlé Toll House Cookie Dough bars, tubs and tube-shaped “chubs.” These products were distributed in the continental U.S. and Puerto Rico.

Not impacted by this recall are the following products: Nestlé Toll House Morsels, Nestlé Toll House Ice Cream Sandwiches, Nestlé Toll House Edible Cookie Dough, and Nestlé Professional SKUs.
The recall is limited only to the ready-to-bake refrigerated products below, with batch codes that begin with 9189 through batch codes that begin with 9295.
Simply Delicious Nestlé Toll House Chocolate Chip Cookie Dough (18oz)
Simply Delicious Nestlé Toll House Peanut Butter Chocolate Chip Cookie Dough (18oz)
Simply Delicious Nestlé Toll House Sugar Cookie Dough (18oz)
Nestlé Toll House Chocolate Chip Chub (16.5oz)
Nestlé Toll House Chocolate Chip Chub (30oz)
Nestlé Toll House Chocolate Chip Lovers Club Tub (80oz)
Nestlé Toll House Chocolate Chip Tub (36oz)
Nestlé Toll House Chocolate Chip Tub (80oz)
Nestlé Toll House Fall’n Leaves Cookie Dough (16oz)
Nestlé Toll House Frozen II Cookie Dough (14oz)
Nestlé Toll House Holiday Chocolate Chip Tree Sprinkle (16oz)
Nestlé Toll House Monster Munch (16oz)
Nestlé Toll House Pinch of Grinch Cookie Dough (14oz)
Nestlé Toll House Triple Chip Cookie Dough Bar (16oz)
Nestlé Toll House Ultimate Chocolate Chip Lovers (16oz)
Nestlé Toll House Ultimate Turtles Cookie Bar (16oz)
Nestlé Toll House White Chip Macadamia Nut (16oz)
Nestlé Toll House Chocolate Chip Bar (16.5oz)
Nestlé Toll House Mini Chocolate Chip Bar (16.5oz)
Nestlé Toll House Peanut Butter Chocolate Chip Bar (16oz)
Nestlé Toll House Sugar Cookie Bar (16.5oz)
Nestlé Toll House Oatmeal Raisin Cookie Bar (16.5oz)
Nestlé Toll House Peanut Butter Cookie Bar (16oz)
M&M’S® Everyday Cookie Dough (14oz)
M&M’S® Ghouls Mix Cookie Dough (14oz)
M&M’S® Holiday Cookie Dough (14oz)
Batch codes can be identified on the product packaging. Please utilize reference images below and look for the four-digit batch code after the “use or freeze-by” date and before the number 5753. Additional product information is available here
External Link Disclaimer
.
Product Names
Impacted Batch Codes
Ready-to-Bake Refrigerated Cookie Dough Bars
9189 through 9295
Ready-to-Bake Refrigerated Cookie Dough Tubs
9189 through 9295
Ready-to-Bake Refrigerated Cookie Dough “Chubs”
9189 through 9295
Nestlé USA is taking this action out of an abundance of caution after receiving reports of food-grade pieces of rubber in some of these products. We have identified the source of the rubber and have already fixed the issue.
No illnesses or injuries have been reported that required medical treatment.
Consumers who may have purchased the products listed above should not prepare or consume them but should instead discard the product. Please retain your proof of purchase and contact Nestlé Consumer Services at nestleproductinquiry@casupport.com.
The quality, safety and integrity of our products remain our number one priority. We sincerely apologize for any inconvenience this action represents to both our consumers and retail customers.
We are working with the U.S. Food & Drug Administration (FDA) on this voluntary recall and will cooperate with them fully.
For consumer support and product questions please call 1-800-681-1676, which will be available 24/7, or email nestleproductinquiry@casupport.com.

• Mylan Pharmaceuticals Inc. is conducting a voluntary nationwide recall of one lot (see table below) of Alprazolam Tablets, USP C-IV 0.5 mg, to the consumer/user level. This lot is being recalled due to the potential presence of foreign substance. Clinical impact from the foreign material, if present, is expected to be rare, but the remote risk of infection to a patient cannot be ruled out. To date, Mylan has not received any adverse events related to this batch.
  Alprazolam Tablets are indicated for the management of anxiety disorder, the short-term relief of symptoms of anxiety, and the treatment of panic disorder, with or without agoraphobia.
  Alprazolam Tablets, USP C-IV 0.5 mg, are packaged in bottles of 500. This batch was distributed in the U.S. between July 2019 and August 2019. The recalled lot is as follows:
  NDC
  Product Description and Strength
  Size
  Lot number
  Expiry
  0378-4003-05
  Alprazolam Tablets, USP C-IV 0.5 mg
  Bottles of 500
  8082708
  September 2020
  Mylan has notified its distributors and customers by letter and is arranging for return of all recalled products. Following are actions for wholesalers, retailers and consumers:
  Wholesaler: Immediately examine your inventory, quarantine and discontinue distribution of these lots. In addition, if you have further distributed the product, please identify your retail level customers and provide a list of customers via Microsoft excel file to mylan5924@stericycle.com within 10 business days. Stericycle will notify your retail level customers that received the affected batches.
  Retailer: Immediately examine your inventory, quarantine and discontinue distribution of these lots. Additionally, if you have further distributed the product, please identify the consumer and notify them immediately of this product recall. The consumer should be instructed to contact Stericycle at 1-888-843-0255 for the documentation packet to return the product.
  Consumer: Please contact Stericycle at 1-888-843-0255 for the documentation packet to return product to Stericycle.
  Consumers with questions regarding this recall can contact Mylan Customer Relations at 800.796.9526 or customer.service@mylan.com, Monday through Friday from 8 a.m. – 5 p.m. EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
  Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
  Complete and submit the report Online
  Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
• OSI Industries, LLC, a Fort Atkinson, Wisc. establishment, is recalling approximately 4,218 pounds of ready-to-eat beef patty products that may be contaminated with extraneous materials, specifically metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The frozen, ready-to-eat beef patty items were produced on August 10, 2019. The following products are subject to recall: [View label (PDF only)]
  38-lb. bulk lined boxes of frozen, ready-to-eat “CHAR-BROILED BEEF PATTIES (CARAMEL COLOR ADDED)” with lot code 22219.
  The products subject to recall bear establishment number “EST. 1300” inside the USDA mark of inspection. These items were shipped to firms that further process the product in Iowa and Wisconsin.
  The problem was discovered during further processing activities at another federal establishment.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  FSIS is concerned that some product may be in freezers of firms that further process the product. Further processing firms that have purchased the product are urged not to distribute them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Consumers with questions regarding the recall can contact OSI Industries, LLC, toll-free, at 855-206-1934. Members of the media with questions regarding the recall can contact Katie Whitmore, Media Coordinator at OSI Industries, at (773) 677-8940.
• Novitium Pharma LLC (Novitium) is voluntarily recalling all quantities and lots, within expiry, of Ranitidine Hydrochloride Capsules in the US to the consumer level. Ranitidine Hydrochloride Capsules are being recalled because of potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA. To date, Novitium has not received any reports of adverse events related to use of the product as part of this recall. Novitium, Navya Jaikumar
  (609) 469-5920
  Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables.
  Ranitidine Hydrochloride Capsules are indicated for the treatment of duodenal ulcer, benign gastric ulcer, reflux esophagitis, post-operative peptic ulcer, Zollinger-Ellison Syndrome, and other conditions where reduction of gastric secretion and acid output is desirable. The affected Ranitidine Hydrochloride Capsule can be identified by NDC numbers stated on the product label.
  Description
  Strength
  Type
  Pack SizeNDC
  Ranitidine Capsules 150mg
  150 mg
  Rx
  60 ct bottle
  70954-001-20
  Ranitidine Capsules 150mg
  150 mg
  Rx
  500 ct bottle
  70954-001-40
  Ranitidine Capsules 300mg
  300 mg
  Rx
  30 ct bottle
  70954-002-10
  Ranitidine Capsules 300mg
  300 mg
  Rx
  100 ct bottle
  70954-002-40
• North Bay Produce, Inc. of Traverse City, Michigan is voluntarily recalling 2,297 cases and 2 bulk bins of fresh apples due to the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  Recalled varieties include McIntosh, Honeycrisp, Jonathan, Fuji, Jonamac and Red Delicious apples. Recalled apples were sold in plastic bags under the brands; Great Lakes, North Bay Produce Pure Michigan as well as unbranded in clear plastic tote bags, white paper tote bags, and individually from retailers display trays. The recalled apples were shipped between October 16th, 2019 and October 21st, 2019 from one North Bay facility to wholesalers, retailers and brokers in Florida, Illinois, Kentucky, Louisiana, Michigan, North Carolina, Texas and Wisconsin.
  Apples purchased at retail prior to October 16th are not affected by this recall, and no other North Bay Produce products are affected by this recall. At this time, we are not aware of any illnesses linked by health officials to this recall.
  Consumers can identify the recalled product by the following product descriptions and photos below:
  < <
  Distributed By
  Variety, Brand & Packaging
  Arrival Date(s)
  UPC Code
  PLU
  Number
  Item
  Number
  Shipped-To- Location
  North Bay
  Produce, Inc.
  McIntosh Great
  Lakes 3lb. Plastic
  Bag, Product of MIUSA
  Delivered between 10/19/19 and 10/21/19
  8 13635
  01012 8Michigan Louisiana
  North Bay
  Produce, Inc.
  Jonathan
  Great Lakes 3lb. Plastic Bag, Product of MI-USA
  Delivered 10/21/19
  8 13635
  01017 3Louisiana
  North Bay
  Produce, Inc.
  Honeycrisp Great
  Lakes 3lb. Plastic
  Bag, Product of MI-
  Delivered 10/21/19
  8 13635
  01018 0LouisianaUSANorth Bay
  Produce, Inc.
  Jonamac Great
  Lakes 3lb. Plastic
  Bag, Product of MIUSA
  Delivered 10/16/19
  8 13635
  01019 7Wisconsin
  North Bay
  Produce, Inc.
  McIntosh North Bay Pure Michigan 3lb. Plastic Bag, Product of MI-USA
  Delivered 10/21/19
  8 13635
  01012 8Michigan
  North Bay
  Produce, Inc.
  Honeycrisp North
  Bay Pure Michigan
  2lb. Plastic Bag,
  Product of MI-USA
  Delivered 10/19/19
  8 13635
  01130 9Michigan
  North Bay
  Produce, Inc.
  Honeycrisp Quarter
  Peck Paper Tote
  Bag, Product of MIUSA
  Delivered 10/19/19700116
  Michigan
  North Bay
  Produce, Inc.
  Fuji
  Half Peck Plastic Tote Bags, Product of MI-USA
  Delivered 10/18/194195All Fresh Thyme
  Farmers Market
  Stores
  North Bay
  Produce, Inc.
  Jonathan Bulk 600lb
  Corugated Bins,
  Product of MI-USA
  Delivered 10/16/19

  Michigan

  North Bay
  Produce, Inc.
  Mcintosh
  Distributed in trays;
  Product of MI-USA
  Delivered
  10/19/19 &
  10/21/19

  4019

  Not sold at retail
  North Bay
  Produce, Inc.
  Red Delicious Distributed in trays; sold individually for retail sale, Product of MI-USA
  Delivered 10/21/19

  4168
  4167

  North Carolina
  Department of
  Agriculture (Food
  Distribution
  Division- Butner)
  Creedmoor, North Carolina
  Feeding South
  Florida
  Pembroke Park,
  Florida
  Anyone who has the recalled product in their possession should not consume it. The product should be discarded or returned to the place of purchase.
  The recall was initiated as a result of a finished product test that indicated the presence of the organism. Upon notification, we immediately ceased the production and distribution product from the identified facility and continue our investigation as to what caused the issue, in cooperation with FDA.
  We have notified our commercial customers to whom we shipped the recalled product and are working with them to remove recalled product from commerce.
  Consumers with questions may call 1-231-929-4001, Monday-Friday, 8am – 5pm Easter

• Lannett Company, Inc. today announced that it is voluntarily recalling all lots within expiry of Ranitidine Syrup (Ranitidine Oral Solution, USP), 15mg/mL to the consumer level due to levels of N-Nitrosodimethylamine (NDMA) above the levels recently established by the FDA for Ranitidine Hydrochloride Syrup (Ranitidine Oral Solution, USP). Lannett was notified by FDA of the potential presence of NDMA on September 17, 2019 and immediately commenced testing of the Active Pharmaceutical Ingredient (API) and drug product. The analysis confirmed the presence of NDMA.
  Risk Statement: NDMA is classified as a probable human carcinogen, a substance that can cause cancer, based on laboratory testing. NDMA is also a known environmental contaminant found in water and foods, including meats, dairy and vegetables.
  The product is used as a short-term treatment for active duodenal ulcers, maintenance therapy for duodenal ulcer patients, treatment of pathological hypersecretory conditions, short-term treatment of active, benign gastric ulcers, maintenance therapy for gastric ulcers, treatment of GERD and treatment of endoscopically diagnosed erosive esophagitis and is packaged in bottles of 16 fluid ounces (one pint) (NDC 54838-550-80). The affected Ranitidine Syrup lots include the following:
  NDC Code
  Batch
  Expiration Date
  NDC Code
  Batch
  Expiration Date
  54838-550-80
  1503A
  10/2019
  54838-550-80
  1646A
  02/2020
  54838-550-80
  1504A
  10/2019
  54838-550-80
  1647A
  02/2020
  54838-550-80
  1505A
  10/2019
  54838-550-80
  1668A
  03/2020
  54838-550-80
  1523A
  10/2019
  54838-550-80
  1669A
  03/2020
  54838-550-80
  1524A
  10/2019
  54838-550-80
  1670A
  03/2020
  54838-550-80
  1525A
  11/2019
  54838-550-80
  1708A
  03/2020
  54838-550-80
  1561A
  12/2019
  54838-550-80
  1709A
  04/2020
  54838-550-80
  1562A
  12/2019
  54838-550-80
  1710A
  04/2020
  54838-550-80
  1563A
  12/2019
  54838-550-80
  1729A
  04/2020
  54838-550-80
  1589A
  12/2019
  54838-550-80
  1730A
  04/2020
  54838-550-80
  1590A
  12/2019
  54838-550-80
  1731A
  04/2020
  54838-550-80
  1591A
  12/2019
  54838-550-80
  1757A
  05/2020
  54838-550-80
  1614A
  01/2020
  54838-550-80
  1758A
  05/2020
  54838-550-80
  1615A
  01/2020
  54838-550-80
  1759A
  05/2020
  54838-550-80
  1617A
  01/2020
  54838-550-80
  1773A
  06/2020
  54838-550-80
  1644A
  02/2020
  54838-550-80
  1774A
  06/2020
  54838-550-80
  1775A
  06/2020
  54838-550-80
  1989A
  12/2020
  54838-550-80
  1794A
  06/2020
  54838-550-80
  1990A
  12/2020
  54838-550-80
  1795A
  06/2020
  54838-550-80
  1991A
  12/2020
  54838-550-80
  1796A
  06/2020
  54838-550-80
  1998A
  01/2021
  54838-550-80
  1817A
  06/2020
  54838-550-80
  1999A
  01/2021
  54838-550-80
  1818A
  07/2020
  54838-550-80
  2000A
  01/2021
  54838-550-80
  1819A
  07/2020
  54838-550-80
  2019A
  01/2021
  54838-550-80
  1840A
  08/2020
  54838-550-80
  2020A
  01/2021
  54838-550-80
  1840B
  08/2020
  54838-550-80
  2065A
  03/2021
  54838-550-80
  1841A
  08/2020
  54838-550-80
  2066A
  03/2021
  54838-550-80
  1842A
  08/2020
  54838-550-80
  2067A
  03/2021
  54838-550-80
  1863A
  08/2020
  54838-550-80
  2071A
  03/2021
  54838-550-80
  1864A
  09/2020
  54838-550-80
  2072A
  03/2021
  54838-550-80
  1865A
  09/2020
  54838-550-80
  2073A
  03/2021
  54838-550-80
  1899A
  10/2020
  54838-550-80
  2076A
  03/2021
  54838-550-80
  1900A
  10/2020
  54838-550-80
  2077A
  03/2021
  54838-550-80
  1901A
  10/2020
  54838-550-80
  2078A
  03/2021
  54838-550-80
  1910A
  10/2020
  54838-550-80
  2126A
  05/2021
  54838-550-80
  1911A
  10/2020
  54838-550-80
  2127A
  05/2021
  54838-550-80
  1912A
  10/2020
  54838-550-80
  2128A
  05/2021
  54838-550-80
  1918A
  10/2020
  54838-550-80
  2164A
  06/2021
  54838-550-80
  1919A
  10/2020
  54838-550-80
  2165A
  06/2021
  54838-550-80
  1920A
  10/2020
  54838-550-80
  2166A
  06/2021
  54838-550-80
  1925A
  10/2020
  54838-550-80
  2179A
  06/2021
  54838-550-80
  1926A
  10/2020
  54838-550-80
  2180A
  07/2021
  54838-550-80
  1927A
  10/2020
  54838-550-80
  2181A
  07/2021
  54838-550-80
  1977A
  12/2020
  54838-550-80
  2214A
  08/2021
  54838-550-80
  1978A
  12/2020
  54838-550-80
  2215A
  08/2021
  54838-550-80
  1979A
  12/2020
  54838-550-80
  2216A
  08/2021
  The product can be identified by NDC number and batch numbers provided above. Ranitidine Syrup was distributed nationwide to wholesalers/distributors.
  Lannett is notifying its distributors and customers via email and via the Lannett website, and is arranging for return of all recalled products. Wholesalers and distributors (direct customers of Lannett) that have Ranitidine which is being recalled should contact Lannett customer service for instructions with regard to returning any remaining stock to Lannett.
  Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
  Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
  Complete and submit the report Online
  Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
• George’s Prepared Foods, a Caryville, Tenn. establishment, is recalling approximately 6,444 pounds of ready-to-eat (RTE) pork sausage patty and turkey sausage patty products that may be contaminated with Salmonella, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The ready-to-eat pork and turkey sausage patty items were produced on April 19, 2019, April 27, 2019, May 7, 2019 and May 9, 2019. The following products are subject to recall: [View Labels (PDF only)]
  24.92-oz. packages containing “Great Value Fully Cooked Original Pork Sausage Patties” with use by date of 10/16/19 and lot code 1091971894.
  24.92-oz. packages containing “Great Value Fully Cooked Original Breakfast Turkey Patties” with use by date of 10/24/19 and lot code 1171971897.
  35.6-oz. packages containing “Family Size Great Value Fully Cooked Original Pork Sausage Patties” with use by date of 11/03/19 and lot code 1271972894 or use by date 11/05/19 and lot code 1291972894.
  The products subject to recall bear establishment number “EST. M2206T or P-2260T” printed on the package. These items were shipped to retail locations nationwide.
  The problem was discovered when the firm notified FSIS that the firm’s third-party cold storage facility had inadvertently shipped the ready-to-eat products to commerce.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  Consumption of ready-to-eat food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 12 to 72 hours after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop a severe illness. Individuals concerned about an illness should contact their health care provider.
  FSIS is concerned that some product may be frozen and in consumers’ refrigerators or freezers or both. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Media and consumers with questions regarding the recall can contact George’s Prepared Foods’ Customer Care Line at (800) 471-9665.
• T & R Enterprise USA Inc., a St. Louis, Mo. establishment, is recalling approximately 126,000 pounds of meat and poultry egg roll products that were produced and packed under insanitary conditions, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The meat and poultry egg roll items were produced on various dates from Aug. 1, 2019 to Sept. 26, 2019. The following products are subject to recall: [View Labels (PDF only)]
  Cases containing 80/2-oz pieces of “SILVER LABEL PORK & VEGETABLE PROTEIN EGG ROLL.”
  Cases containing 120/2-oz pieces of “Dai Kin PORK & TEXTURED VEGETABLE PROTEIN EGG ROLL.”
  Cases containing 120/2-oz pieces of “TITA’S PORK & TEXTURED VEGETABLE PROTEIN EGG ROLL.”
  Cases containing 120/2-oz pieces of “TITA’S CHICKEN & TEXTURE VEGETABLE PROTEIN EGG ROLL.”
  Cases containing 120/2-oz pieces of “WORLD CUISINE PORK & TEXTURED VEGETABLE PROTEIN EGG ROLL.”
  Cases containing 120/2-oz pieces of “WORLD CUISINE CHICKEN & TEXTURED VEGETABLE PROTEIN EGG ROLL.”
  The products subject to recall bear establishment number “EST. 33792” or “P33792” inside the USDA mark of inspection. These items were shipped to institutional locations in Georgia and Missouri.
  The problem was discovered while FSIS was conducting routine food inspection activities.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  FSIS is concerned that some product may be frozen and in consumers’ refrigerators or freezers or both. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Media and consumers with questions regarding the recall can contact Howard Lin, Manager, T & R Enterprise USA Inc., at (404) 955-2096.
• Taylor’s Sausage Inc., a Cave Junction, Ore. establishment, is recalling approximately 641 pounds of ready-to-eat meat and poultry sausage products because the products may be misbranded and contain a pork casing or a sheep casing that were not declared on the product label, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The ready-to-eat meat and poultry sausage items were packaged on June 26, 2019, Aug. 6, 2019, Aug. 16, 2019, Sept. 5, 2019 and Oct. 10, 2019. The following products are subject to recall: [View labels (PDF only)]
  16-oz. vacuum-sealed packages containing fully cooked, ready-to-eat, “TAYLOR’S Sausage Smoked Chicken and Apple Sausage” with lot code numbers 19217, 19176 and 19282.
  16-oz. vacuum-sealed packages containing fully cooked, ready-to-eat, “TAYLOR’S Sausage Cheddar Dogs” with lot code numbers 19247 and 19217.
  The products subject to recall bear establishment number “6172” or “P-6172” inside the USDA mark of inspection. These items were sold at retail locations in California and Oregon.
  The problem was discovered by FSIS during routine inspection activities.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers.
  Consumers with questions about the recall can contact Yvette Pendleton, shipping and receiving manager at Taylor’s Sausage Inc., at (541) 592-4185. Members of the media with questions about the recall can contact Emily Nichols, co-owner of Taylor’s Sausage Inc., at (541) 592-4185.
• UNFI is voluntarily recalling cases of Arla Apetina Marinated Feta & Olives in Oil, Pitted distributed by UNFI. The product requires refrigeration to ensure food safety and we have learned that some product distributed to retail customers from 2 UNFI distribution centers may have been exposed to temperatures above refrigeration during storage and/or distribution by UNFI’S customers. Extended exposure to above-refrigerated temperatures may allow growth of bacteria such as Clostridium Botulinum to reach unsafe levels, which if consumed can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled. No illnesses, including allergic reactions, involving this product have been reported to date in connection with this problem.
  Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these symptoms should seek immediate medical attention.
  A total of 75 cases of this product were distributed to 69 retail customers serviced by UNFI distribution centers in Greenwood, IN. and Sarasota, Fla. between Jan. 1, 2019 and Aug. 30, 2019 to the following states IN, KY, IL, MI, FL, OH, MO. No other distribution centers or products in states that are not listed are impacted by this notice. Additionally, Arla Apetina Marinated Feta & Olives in Oil, not sold by UNFI Greenwood or Sarasota are not impacted by UNFI’s voluntary recall.
  The product comes in a 3.1-pound plastic package marked with UPC code 9393605697.
  Retailers who have purchased the Arla Apetina Marinated Feta & Olives in Oil, Pitted product from these two distribution centers should remove any remaining product from the supply chain and discard the product in a manner that would prevent its consumption or distribution and contact their UNFI account managers for a full refund. Consumers with questions may contact the company at 800-451-2525.
• Jumbo Foods Inc. of Mukilteo, WA has issued a voluntary recall of Tuscan Sun (TS) brand chicken salad sandwiches, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
  The following affected sandwiches products were distributed exclusively by Jumbo Foods Inc to food service and retail stores in Arizona, California, Nevada, North Carolina, Oregon, Utah, Virginia, and Washington.
  FROZEN Product
  UPC
  Codes on Pkg
  Sell By/ Use By Dates
  Distribution Dates
  TS Bacon Ranch Chicken Salad on 9 grain
  4370101417
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  TS Cranberry Chicken Salad on 9 grain
  4370101414
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  TS Chipolte Chicken Salad on 9 grain
  4370101415
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  TS Chicken Salad on 9 grain
  4370101413
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  TS Chicken Salad Wedges
  4370101426
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  REFRIGERATED product
  UPC
  Codes on Pkg.
  Sell By/ Use By Dates
  Distribution Dates
  TS Bacon Ranch Chicken Salad on 9 grain
  4370101417
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  TS Cranberry Chicken Salad on 9 grain
  4370101414
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  TS Chipolte Chicken Salad on 9 grain
  4370101415
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  TS Chicken Salad on 9 grain
  4370101413
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  TS Chicken Salad Wedges
  4370101426
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  Jumbo Foods Inc began shipping these frozen or refrigerated sandwiches products between March 11, 2019 and September 27, 2019. Frozen sandwiches have no sell by or use by date printed on packages and have 8 months shelf life. Frozen products will be thawed, and the expiry dates are applied at stores. Refrigerated sandwiches distributed by Jumbo Foods have 28 days shelf life and the sell by or use by date stickers are observed on packages.
  This recall was brought to our attention by The Suter Company whose poultry supplier Tip Top Poultry has issued a voluntary recall of ready-to-eat (RTE) poultry products that may be adulterated with Listeria monocytogenes.
  No illnesses have been reported to date in relation to these products or recall.
  This recall is being made with the knowledge of the U.S. Food and Drug Administration.
  Consumers who have purchased these recalled products should not consume them. Consumers should discard the products or return them to the point of purchase. Consumers with questions should call Jumbo Foods Inc. Customer Service at 800-562-6507, 8:15 am – 4:30 pm, PST, Monday through Friday.

• Sanofi on Friday, October 18, initiated a voluntary recall of all Zantac OTC (over-the-counter) in the United States. This includes Zantac 150®, Zantac 150® Cool Mint, and Zantac 75®. Zantac tablets are an oral, over-the-counter product to prevent and relieve heartburn associated with acid ingestion and sour stomach.
  On September 13, 2019, the U.S Food and Drug Administration issued a public statement alerting that some ranitidine medicines, including Zantac OTC, could contain NDMA at low levels and asked manufacturers to conduct testing.
  Evaluations are ongoing on both drug substance (active ingredient) and finished drug product. Due to inconsistencies in preliminary test results of the active ingredient used in the U.S. products, Sanofi has made the decision to conduct the voluntary recall as the investigation continues.
  Active ingredients used in Sanofi’s ranitidine products outside of the U.S. and Canada are sourced from different suppliers. Sanofi has also issued a voluntary recall in Canada. The company is committed to transparency and will continue to communicate results with health authorities from the ongoing testing, and work with them to make informed decisions based on available data and evidence.
  Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables.
  Sanofi will be notifying its distributors and customers via email and via the Sanofi web site, and will arrange for return of all recalled products. Wholesalers (direct customers) will be asked to immediately stop distribution and return any stock to Sanofi, and contact the retail outlets in their group to do the same. Retailers will be asked to immediately stop dispensing Zantac tablets and return remaining stock to Sanofi by contacting INMAR at 877-275-0993 (option 1) or via fax at 336-499-8145 or email at zantacrecall@inmar.com. Consumers are asked to speak to their physician or pharmacist about alternate heartburn relief options.
  Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
  Complete and submit the report Online
  Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
• : Perrigo Company plc announced that it has initiated a voluntary, worldwide product recall to the retail customer level of ranitidine (all pack sizes). The recall is being taken due to possible presence of a nitrosamine impurity called NDMA. NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests.After regulatory bodies announced that ranitidine may potentially contain NDMA, Perrigo promptly began testing of its externally sourced ranitidine API (active pharmaceutical ingredient) and ranitidine-based products. On October 8, 2019, Perrigo halted shipments of the product based upon preliminary results. Based on the totality of data gathered to date, Perrigo has made the decision to conduct this voluntary recall.RECOMMENDATION:
  Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.Healthcare providers and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:
  • Complete and submit the report online.
  • Download form or call 1-800-332-1088 to request a reporting form, then complete
• Dr. Reddy’s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, along with its subsidiaries, together referred to as “Dr. Reddy’s”) confirms it had intiatiated a voluntary nationwide recall on October 1, 2019, (at the retail level for over-the-counter products and at the consumer level for prescription products) of all of its ranitidine medications sold in US due to confirmed contamination with N-Nitrosodimethylamine (NDMA) above levels established by the FDA. This recall follows the USFDA’s caution note alerting patients and health care professionals that NDMA was found in certain samples of ranitidine. To date, Dr. Reddy’s has not received any reports of adverse events related to the recall of Dr. Reddy’s Ranitidine products. The recall includes all quantities in the US that are within expiry.
  Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables.
  Ranitidine is available as an over-the-counter (OTC) and prescription drug. Over-the-counter (OTC) ranitidine tablets are used to relieve heartburn associated with acid indigestion and sour stomach. OTC Ranitidine Tablets are also used to prevent heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages. Prescription ranitidine capsules are prescribed for the short-term treatment of active duodenal ulcer; maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers; treatment of pathological hypersecretory conditions (eg, Zollinger-Ellison syndrome and systemic mastocytosis); short-term treatment of active, benign gastric ulcer; maintenance therapy for gastric ulcer patients at reduced dosage after healing of acute ulcers; treatment of GERD (Gastroesophageal reflux disease); treatment of endoscopically diagnosed erosive esophagitis; and for maintenance of healing of erosive esophagitis.
  Dr. Reddy’s Ranitidine products can be identified by NDC numbers on the product label. All Ranitidine products with expiration dated September 2019 to June 2021 are being recalled:
  Description
  Strength
  Type
  Pack
  NDC
  Ranitidine Capsules 150mg, 60
  150 mg
  Rx
  60 ct bottle
  5511112960
  Ranitidine Capsules 150mg, 500
  150 mg
  Rx
  500 ct bottle
  5511112905
  Ranitidine Capsules 300mg, 30
  300 mg
  Rx
  30 ct bottle
  5511113030
  Ranitidine Capsules 300mg, 100
  300 mg
  Rx
  100 ct bottle
  5511113001
  Rantidine Tablets, USP 150mg,190(2×95)Tray (Sam’s Club)
  150 mg
  OTC
  190 ct (2×95) tray
  150062076
  (UPC Code 078742089720)
  Ranitidine Tablets, USP 150mg, 95 (Walgreens)
  150 mg
  OTC
  95 ct bottle
  0363-0010-62
  Ranitidine Tablets, USP 150 mg 220 CT Btl (Walmart)
  150 mg
  OTC
  220 ct bottle
  49035-404-65
  Ranitidine Tablets, USP 150mg 50ct Btl (Kroger)
  150 mg
  OTC
  50 ct bottle
  30142-505-50
  Ranitidine Tablets, USP 150mg 24ct Btl (Kroger)
  150 mg
  OTC
  24 ct bottle
  30142-505-34
  Ranitidne Tablets, USP 150mg 65 Ct Btl (Walgreens)
  150 mg
  OTC
  65 ct bottle
  0363-0010-61
  Ranitidine Tablets, USP 150 TAB 65ct BTL CP32 (Walmart)
  150 mg
  OTC
  65 ct bottle
  49035-404-61
  Ranitidine Tablets, USP 150 Tab 200Ct Btl (Walgreens)
  150 mg
  OTC
  200 ct bottle
  0363-0010-01
  Ranitidine Tablets, USP 150mg Tabs Btl, 24 (Walgreens)
  150 mg
  OTC
  24 ct bottle
  0363-0010-34
  Ranitidine Tablets, USP 75 TAB 30ct Bottle NG (CVS)
  75 mg
  OTC
  30 ct bottle
  69842-871-30
  Ranitidine Tablets, USP 75mg Tab 30Ct Btl (Walgreens)
  75 mg
  OTC
  30 ct bottle
  0363-0131-30
  Ranitidine Tablets, USP 75mg Tab 80Ct Btl (Walgreens)
  75 mg
  OTC
  80 ct bottle
  0363-0131-80
  Ranitidine Tablets, USP 75 TAB 80ct Bottle NG (CVS)
  75 mg
  OTC
  80 ct bottle
  69842-871-80
  Ranitidine Tablets, USP 75 TAB 160ct Bottle NG (CVS)
  75 mg
  OTC
  160 ct bottle
  69842-871-37
  Ranitidine Tablets, USP 75mg 30ct Btl (Kroger)
  75 mg
  OTC
  30 ct bottle
  30142-131-30
  Ranitidine Tablets, USP 150 TAB 24ct BTL (CDMA)
  150 mg
  OTC
  24 ct bottle
  63868-480-24
  Ranitidine Tablets, USP 150 Tablet 130ct Bottle NV (Walmart)
  150 mg
  OTC
  130 ct bottle
  49035-404-13
  Ranitidine Tablets, USP 150 TAB 50ct BTL (CDMA)
  150 mg
  OTC
  50 ct bottle
  63868-480-50
  Ranitidine Tablets, USP 75 Tab 60ct Btl (Dr. Reddy’s)
  75 mg
  OTC
  60 ct bottle
  55111-131-60
  Ranitidine Tablets, USP 75 TAB 60ct BTL (CDMA)
  75 mg
  OTC
  60 ct bottle
  63868-482-60
  Ranitidine Tablets, USP 75 TAB 30ct BTL (CDMA)
  75 mg
  OTC
  30 ct bottle
  63868-482-30
  Ranitidine Tablets, USP 150mg Tablets 24ct BTL00 (Dr. Reddy’s)
  150 mg
  OTC
  24 ct bottle
  55111-404-34
  Ranitidine Tablets, USP 150 Tab 95ct Btl (HCA)
  150 mg
  OTC
  95 ct bottle
  43598-808-62
  Ranitidine Tablets, USP 150 Tab 220ct Btl (HCA)
  150 mg
  OTC
  220 ct bottle
  43598-808-65
  Ranitidine Tablets, USP Tab 150mg 40ct Bottle (Target)
  150 mg
  OTC
  40 ct bottle
  11673-849-40
  Ranitidine Tablets, USP 150 Tab 24ct Btl (Thirty Madison)
  150 mg
  OTC
  24 ct bottle
  71713-203-02
  Ranitidine Tablets, USP 150 Tab 95ct Btl (Thirty Madison)
  150 mg
  OTC
  95 ct bottle
  71713-203-05
  Ranitidine Tablets, USP 75mg (GeriCare)
  75 mg
  OTC
  All counts
  57896-715
  Ranitidine Tablets, USP 150mg (GeriCare)
  150 mg
  OTC
  All counts
  57896-717
  If consumers have questions regarding this recall or to report an adverse event, please contact the Company’s Medical Information Call Center at 1-888-375-3784 (1-888-DRL-DRUG) between the hours of 8 a.m. to 8 p.m. ET, Monday through Friday. Patients should contact their healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality concerns experienced with the use of this product may also be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online, Regular Mail or Fax: Download Form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.
• Newport Beach, California. GL Holdings is voluntarily recalling six lots of Green Lumber 2-, 4-, and 10-capsule packages purchased on or before August 10, 2019 to the consumer level. FDA analysis has found one lot of Green Lumber distributed between June and August 2019 to be tainted with tadalafil.
  Consumption of a product with undeclared tadalafil may pose a risk to consumers who take prescription medications containing nitrates (such as nitroglycerin). The combination of tadalafil and nitrates may lower blood pressure to dangerous levels which can be life threatening. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates and may be the population most likely to be affected. To date, GL Holdings has not received any reports of adverse events related to this recall.
  GL Holdings is recalling the lot that tested positive for tadalafil and, out of an abundance of caution, GL Holdings is also recalling all previous lots, thus this recall encompasses all Green Lumber products sold on or before August 10, 2019. Tadalafil is an FDA approved drug for the treatment of erectile dysfunction. The presence of tadalafil in the Green Lumber products renders them unapproved drugs for which safety and efficacy have not been established, and therefor subject to recall.
  The Green Lumber product is marketed as dietary supplements for male sexual enhancement and is packaged in 2-, 4-, and 10-capsule blister packs.
  The Green Lumber lot that tested positive for tadalafil was sold between June 10 and August 10, 2019. Some of the blister packs are marked with “XC06 EXP 06/2022.” It is sold in a white wrapper with a green Green Lumber logo on the front and has one of the following UPC codes:
  2 pack: X0020TSV4R
  4 pack: X0020TRRHJ
  10 Pack: X0020TUJLZ
  Other lots that are being recalled were sold between April 1, 2018 and June 10, 2019 and may have a different UPC code on the package. Some of these blister packages are marked with one of the following “XC12EXP12/2020,” “XC06EXP06/2021,” “XC10EXP10/2021,” “XC02EXP02/2022,” or “XC04EXP04/2022.”
  Images of these packages are included below so that they may be more easily identified by consumers.
  This product was distributed in the United States and Canada via internet sales.
  GL Holdings is notifying its distributors and customers by email and is arranging for replacement of recalled products, at the request of the customer. Consumers with questions regarding this recall can contact GL Holdings via email at recall@greenlumber.com at any time or by phone at 949-426-8622 on Monday through Friday between the hours of 9 a.m. to 5 p.m. Pacific Time.
  Consumers who purchased the product should stop consuming it and return any unused product to GL Holdings. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
  Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
  Complete and submit the report Online: http://www.fda.gov/medwatch/report.htm
  Regular Mail or Fax: Download form http://www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
• Global Zakii Enterprises, LLC, a Houston, Texas establishment, is recalling approximately 100 pounds of canned meat and canned poultry products that were not presented for import re-inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Additionally, the products were imported from Jordan, a country ineligible to export products to the United States.
  The canned meat and canned poultry products were imported on or about September 20, 2019. The following products are subject to recall: [View Labels (PDF Only)]
  800-gm cans containing “UNIUM Chicken Luncheon”.
  800-gm cans containing “UNIUM Luncheon Meat”.
  500-gm cans containing “UNIUM Luncheon Meat”.
  200-gm cans containing “UNIUM Chicken Luncheon”.
  200-gm cans containing “UNIUM Luncheon Meat”.
  340-gm cans containing “BISHAWY Extra CORNED BEEF”.
  7-oz cans containing “TRADE MARK SHARAWI Extra CORNED BEEF PRODUCT OF BRAZIL”.
  These items were shipped to retail locations in Texas.
  The problem was discovered after a consumer complaint, and a subsequent investigation by FSIS.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
  FSIS is concerned that some product may be in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Consumers and members of the media with questions about the recall can contact Khaldoon Barakat, Manager, Global Zakki Enterprises, LLC, at (832) 672-8771.
• Pride of Florida, a Raiford, Fla. establishment, is recalling approximately 64,797 pounds of raw beef products that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The raw ground beef items were produced on various dates from Sept. 23, 2019 to Oct. 10, 2019. The following products are subject to recall: [View Labels (PDF only)]
  24-lb. Case containing 1-lb chubs of “CIRCLE A BRAND 85-15 LEAN GROUND BEEF” with pack date Oct. 8, 2019; package code of Oct. 8. 2020 and case code of 1-86407-30002-5.
  24-lb. Case containing 1-lb chubs of “CIRCLE A BRAND 80/20 GROUND BEEF” with pack dates 9-26-19, 9-27-19, 9-30-19; package codes of Sept. 26, 2020, Sept. 27, 2020, Sept. 30, 2020; and case code of FG-8020-24-1.
  12-lb. Case containing 1-lb chubs of “CIRCLE A BRAND 80/20 GROUND BEEF” with a pack date of 9-26-19; package code of Sept. 26, 2020; and a case code of FG-8020-12-1.
  15-lb. Case containing 20-oz packages of “CLARKS 5 CHOPPED BEEF STEAKS” with a pack date of 9-23-19; a package code of Sept. 23, 2020; and a case code of 0-73673-00211-4.
  13-lb. Case containing 17.5-oz packages of “CLARKS 5 CHOPPED PEPPER STEAKS” with a pack date of 9-23-19; a product code of Sept. 23, 2020; and a case code of 0-73673-00222-0.
  20-lb. Case containing 5.3-oz packages of “SOUTHEAST PROTEIN PURVEYOR GROUND BEEF PATTIES” with a pack date of 10-18-19; a package code of Oct. 10, 2020; and a case code of FG-8020-20-5.3.
  40-lb. Case containing 10-lb packages of “SOUTHEAST PROTEIN PURVEYOR 81/19 GROUND BEEF” with pack dates of 9-30-19, 10-2-19, 10-8-19, package codes of Sept. 30, 2020, Oct. 2, 2020, and Oct. 8, 2020; and case codes of FG-81/19-10C-40# and FG-81/19-10C-40.
  60-lb. Case containing 10-lb packages of “SOUTHEAST PROTEIN PURVEYORS 80-20 GROUND BEEF” with a pack date of 9-26-19; a package code of Sept. 26, 2020; and a case code of FG80/20-60-6/10
  The products subject to recall bear establishment number “EST. 18506” inside the USDA mark of inspection. These items were shipped to commercial distributors and a cold storage warehouse in Florida.
  The problem was discovered when the firm was notified by their third-party laboratory that a sample was positive for E. coli O157:H7, but the products associated with the sample had already been shipped into commerce. There have been no confirmed reports of adverse reactions due to consumption of these products.
  Anyone concerned about an injury or illness should contact a healthcare provider. E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
  FSIS is concerned that some product may be frozen and in Commercial Distributor’s freezers. Distributors who have obtained these products are urged not to distribute them. These products should be thrown away or returned to the place of origin.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160°F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
  Consumers and members of the media with questions about the recall can contact Denise Kiminki, Chief Administrator Officer, Pride Of Florida, at (813) 324-8733.
• MawMaw’s Chicken Pies, a Kernersville, N.C. establishment, is recalling an undetermined amount of chicken pie and meatloaf products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain milk and soy, known allergens, which are not declared on the product label.
  The not-ready-to-eat chicken pie and meatloaf items were produced between Sept. 17, 2019 to Oct. 16, 2019. The products have a one-year shelf life. The following products are subject to recall: [View Labels (PDF only)]
  10-oz. shrink wrapped packages containing “MawMaw’s Chicken Pies NO VEGGIES” with expiration dates ranging from 9/17/19 to 10/16/20.
  10-oz. shrink wrapped packages containing “MawMaw’s Chicken Pies WITH VEGGIES” with expiration dates ranging from 9/17/19 to 10/16/20.
  10-oz. shrink wrapped packages containing “MawMaw’s Chicken Pies NO VEGGIES MAWMAW’S KICKIN’ CHICKEN” with expiration dates ranging from 9/17/19 to 10/16/20.
  33-oz. shrink wrapped packages containing “MawMaw’s Chicken Pies NO VEGGIES” with expiration dates ranging from 9/17/19 to 10/16/20.
  33-oz. shrink wrapped packages containing “MawMaw’s Chicken Pies WITH VEGGIES” with expiration dates ranging from 9/17/19 to 10/16/20.
  33-oz. shrink wrapped packages containing “MawMaw’s Chicken Pies NO VEGGIES MAWMAW’S KICKIN’ CHICKEN” with expiration dates ranging from 9/17/19 to 10/16/20.
  1-lb. shrink wrapped, aluminum tray containing “MawMaw’s Meatloaf” with expiration dates ranging from 9/17/19 to 10/16/20.
  The products subject to recall bear establishment number “EST. 46456” inside the USDA mark of inspection. These items were shipped to retail locations in North Carolina.
  The problem was discovered by FSIS inspectors during routine label verification activities.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  FSIS is concerned that some product may be frozen and in consumers’ refrigerators or freezers or both. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Consumers and members of the media with questions about the recall can contact Julia Brown, owner, MawMaw’s Chicken Pies, at (336) 416-2334.
• MedWatch – The FDA Safety Information and Adverse Event Reporting Program

A MedWatch Safety Alert was just added to the FDA Recalls webpage.

TOPIC: Johnson’s Baby Powder by Johnson & Johnson: Recall – Single Lot: Due to the presence of sub-trace levels of chrysotile asbestos contamination

AUDIENCE: Consumer, Pharmacy

ISSUE: Johnson & Johnson Consumer Inc. announced that it is initiating a voluntary recall in the United States of a single lot (#22318RB) of its Johnson’s Baby Powder. The recall is in response to a FDA test indicating the presence of sub-trace levels of chrysotile asbestos contamination (no greater than 0.00002%) in samples from a single bottle purchased from an online retailer.

RECOMMENDATION: If you or someone you provide care for owns a bottle of Johnson’s Baby Powder Lot #22318RB, discontinue use of the product.

Consumers and health professionals are encouraged to report adverse events or side effects related to the use of this product to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:
• Complete and submit the report online.
• Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the form, or submit by fax to 1-800-FDA-0178.
Read Recall

• T & R Enterprise USA Inc., a St. Louis, Mo. establishment, is recalling approximately 118,000 pounds of meat and poultry egg roll products that were produced and packed under insanitary conditions, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The meat and poultry egg roll items were produced on various dates from Aug. 1, 2019 to Sept. 26, 2019. The following products are subject to recall: [View Labels (PDF only)]
  2-oz. cases containing 80 pieces of “SILVER LABEL PORK & VEGETABLE PROTEIN EGG ROLL.”
  2-oz. cases containing 120 pieces of “Dai Kin PORK & TEXTURED VEGETABLE PROTEIN EGG ROLL.”
  2-oz. cases containing 120 pieces of “TITA’S PORK & TEXTURED VEGETABLE PROTEIN EGG ROLL.”
  2-oz. cases containing 120 pieces of “TITA’S CHICKEN & TEXTURE VEGETABLE PROTEIN EGG ROLL.”
  The products subject to recall bear establishment number “EST. 33792” or “P33792” inside the USDA mark of inspection. These items were shipped to institutional locations in Georgia and Missouri.
  The problem was discovered while FSIS was conducting routine food inspection activities.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  FSIS is concerned that some product may be frozen and in consumers’ refrigerators or freezers or both. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Media and consumers with questions regarding the recall can contact Howard Lin, Manager, T & R Enterprise USA Inc., at (404) 955-2096.
  Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
  USDA Recall Classifications
  Class I
  This is a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.
  Class II
  This is a health hazard
• Mical Seafood, Inc. of Cooper City, FL, has voluntarily initiated an expanded recall of frozen, wild-caught yellowfin Tuna Loins, Tuna Poke, Tuna Steaks, Tuna Ground Meat, and Tuna Saku (products of Vietnam) due to potentially elevated levels of histamine. Elevated levels of histamines can produce an allergic reaction called scombroid fish poisoning that may result in symptoms that can generally appear within minutes to several hours after eating the affected fish.
  The most common symptoms of histamine or scombroid fish poisoning are tingling or burning sensation in the mouth, facial swelling, rash, hives and itchy skin, nausea, vomiting or diarrhea; these symptoms usually resolve within several hours without medical intervention. However, each individual may experience symptoms differently. If symptoms are severe an individual should seek immediate medical attention for treatment.
  These tuna products were wholesaled to customers in: AL, CA, FL, GA, ID, IL, IN, LA, MA, MI, MN, MO, MS, NC, NJ, NV, NY, PA, RI, TX, UT, VA and WI.
  ALL LOTS WITH PRODUCTION DATES: 04/01/2019 TO 05/31/2019
  Production dates can be found on the ends of the Mical Brand master cases. These dates are stamped on to the masters as they are produced.
  BRAND
  DESCRIPTION
  PACK
  ORIGIN
  Mical Seafood
  Tuna Loins AAA 3-5LB IVP
  30 LB
  Vietnam
  Mical Seafood
  Tuna Loins AAA 5-8LB IVP
  30 LB
  VietnaMical Seafood
  Tuna Poke AAA 1.5 cm IVP
  10 LB
  Vietnam
  Mical Seafood
  Tuna Poke AAA 2cm IVP
  10 LB
  VietnamMical Seafood
  Tuna Steaks AAA 4oz, 6oz, 8oz, 10oz IVP
  10 LB
  Vietnam
  Mical Seafood
  Tuna Steaks AA 4oz, 6oz, 8oz, 10oz IVP
  10 LB
  VietnamMical Seafood
  Tuna Ground Meat AAA IVP
  10 LB
  Vietnam
  Mical Seafood
  Tuna Saku AAA 8-12oz IVP
  10 LB
  Vietnam
  Mical Seafood
  Tuna Saku AAA 12-16oz IVP
  10 LB
  Vietnam
  Customers who received products with the listed Production Dates of: 04/01/2019 to 05/31/2019 should not consume them. Inventory should be quarantined until returned to the supplier or to Mical Seafood, Inc.
  Customers with questions or concerns may contact the company’s Recall Team: (Jennifer Gonzalez or Margarita Alzugaray) by calling (954) 935-0133, Monday through Friday, 8 a.m. to 5 p.m., Eastern Time.
• The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for raw non-intact beef products derived from imported beef from Ontario, Canada that has been recalled by Ryding-Regency Meat Packers, Ltd. because it may be contaminated with E. coli O157:H7. The Canadian Food Inspection Agency is conducting a food safety investigation and determined that certain products produced by the company may be contaminated. While Canada is the recalling authority, FSIS is amplifying the recall through this public health alert.
  The Canadian Food Inspection Agency notified FSIS that several shipments of beef implicated in a series of recalls have been exported to the U.S. FSIS has identified that imported beef manufacturing trimmings produced on May 27 and 30, 2019 that are subject to recall were used in the U.S. to produce other raw non-intact beef products distributed for retail sale. The U.S. companies that produced these raw non-intact beef products have received notice of the recall from Ryding-Regency and FSIS has confirmed that they are following the instructions provided to recall affected product from their customers. However, retail consumers may not have received such notification.
  The following products have been identified as part of the Canadian recall and were distributed to institutions and retailers in Connecticut, Illinois, Maine, Massachusetts, New Hampshire, New Jersey, New York, Pennsylvania, Rhode Island, and Vermont: [View Labels (PDF Only)]
  10-lb. cardboard box packages containing bulk plastic wrapped raw frozen ground beef gyros labeled “DEVANCO FOODS CHICAGO’S FAVORITE” GYROS SLICES (STRIPS) with a case code 159 19.
  10-lb. cardboard box packages containing bulk plastic wrapped raw frozen ground beef gyros labeled “KRONOS HALAL GYROS STRIPS” HALAL CERTIFIED BEEF GYROS UNCOOKED, IQF STRIPS with a case code 19 159.
  Retail sized (8 patties) cardboard box packages containing “ZIYAD PREMIUM QUALITY Beef Hamburger Patties” with a case code 911541.021541.
  Retail sized (8 kabobs) cardboard box packages containing “ZIYAD PREMIUM QUALITY Uncooked Kufta Kabob” with a case code 911154.021154.
  8-lb. cardboard box packages containing bulk plastic wrapped raw frozen ground beef patties labeled “Shop Right 100% PURE QUARTER POUND Ground Beef Hamburgers” and a sell by date of 060720.
  3-lb. cardboard box packages containing plastic wrapped raw frozen ground beef patties labeled “Shop Right 100% PURE Ground Beef Hamburgers” and a sell by date of 060720.
  2-lb. cardboard box packages containing plastic wrapped raw frozen ground beef patties labeled “LANDIS BRAND 100% ALL BEEF PATTIES 8 Quarter Pound Patties” and a sell by date of 060720.
  FSIS is concerned that some product may be in institutional or consumers’ freezers. Institutions that have these products are urged not to serve them and consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  E. coli O157:H7 is a potentially deadly bacterium that can cause bloody diarrhea, dehydration, and in the most severe cases, kidney failure. The very young, seniors and persons with weak immune systems are the most susceptible to foodborne illness.FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160° F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
• Kenosha Beef International, a Columbus, Ohio establishment, is recalling an undetermined amount of seasoned beef products that may be contaminated with extraneous materials, specifically metal shavings, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The seasoned beef items were produced on various dates from Sept. 20, 2019 to Oct. 4, 2019. The following products are subject to recall: [View Labels (PDF Only)]
  Cases containing eight 5-lb. plastic bags of “TACO BELL SEASONED BEEF Taco and Burrito Filling” with use by dates of “L2 11/4/19” to “L2 11/18/19”.
  The products subject to recall bear establishment number “EST. 10130” on the case. These items were shipped to five distribution centers, and from there shipped to restaurant locations nationwide.
  The problem was discovered when the firm notified FSIS on Oct. 12, 2019, that it received three customer complaints.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  FSIS is concerned that some product may be in restaurant refrigerators. Restaurants who have purchased these products are urged not to serve them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Consumers and members of the media with questions about the recall can contact Dennis Vignieri, President and CEO, Kenosha Beef International, at (262) 859-2272, ext. 1205.
• A MedWatch Safety Alert was just added to the FDA Recalls web page.TOPIC: Certain Lots of Plum and Sapphire Microbore Infusion Sets with Inline Filters by ICU Medical: Recall – Due to potential for small amounts of fluid leaking out of the air vents on the inline filtersISSUE: ICU Medical announced a voluntary recall on July 29, 2019 of certain lots of Plum and Sapphire Microbore Infusion Sets with inline filters due to the potential for small amounts of fluid leaking out of the air vents on the inline filters.To date, ICU Medical is not aware of adverse events related to this matter and is issuing this notification out of an abundance of caution.Based on complaints the affected product lots, which were distributed nationwide to ICU Medical customers, are listed in the recall.Health care professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:
  • Complete and submit the report online .
  • Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the form, or submit by fax to 1-800-FDA-0178.
  Read Recall
• Jumbo Foods Inc. of Mukilteo, WA has issued a voluntary recall of Tuscan Sun (TS) brand chicken salad sandwiches, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
  The following affected sandwiches products were distributed exclusively by Jumbo Foods Inc to food service and retail stores in Arizona, California, Nevada, North Carolina, Oregon, Utah, Virginia, and Washington.
  FROZEN Product
  UPC
  Codes on Pkg
  Sell By/ Use By Dates
  Distribution Dates
  TS Bacon Ranch Chicken Salad on 9 grain
  4370101417
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  TS Cranberry Chicken Salad on 9 grain
  4370101414
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  TS Chipolte Chicken Salad on 9 grain
  4370101415
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  TS Chicken Salad on 9 grain
  4370101413
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  TS Chicken Salad Wedges
  4370101426
  A11 – E39
  None
  3/11/2019 – 9/27/2019
  REFRIGERATED product
  UPC
  Codes on Pkg.
  Sell By/ Use By Dates
  Distribution Dates
  TS Bacon Ranch Chicken Salad on 9 grain
  4370101417
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  TS Cranberry Chicken Salad on 9 grain
  4370101414
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  TS Chipolte Chicken Salad on 9 grain
  4370101415
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  TS Chicken Salad on 9 grain
  4370101413
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  TS Chicken Salad Wedges
  4370101426
  A11 – E39
  3/21/2019 – 11/01/2019
  3/11/2019 – 9/27/2019
  Jumbo Foods Inc began shipping these frozen or refrigerated sandwiches products between March 11, 2019 and September 27, 2019. Frozen sandwiches have no sell by or use by date printed on packages and have 8 months shelf life. Frozen products will be thawed, and the expiry dates are applied at stores. Refrigerated sandwiches distributed by Jumbo Foods have 28 days shelf life and the sell by or use by date stickers are observed on packages.
  This recall was brought to our attention by The Suter Company whose poultry supplier Tip Top Poultry has issued a voluntary recall of ready-to-eat (RTE) poultry products that may be adulterated with Listeria monocytogenes.
  No illnesses have been reported to date in relation to these products or recall.
  This recall is being made with the knowledge of the U.S. Food and Drug Administration.
  Consumers who have purchased these recalled products should not consume them. Consumers should discard the products or return them to the point of purchase. Consumers with questions should call Jumbo Foods Inc. Customer Service at 800-562-6507, 8:15 am – 4:30 pm, PST, Monday through Friday.
• UNFI is voluntarily recalling cases of Arla Apetina Marinated Feta & Olives in Oil, Pitted distributed by UNFI. The product requires refrigeration to ensure food safety and we have learned that some product distributed to retail customers from 2 UNFI distribution centers may have been exposed to temperatures above refrigeration during storage and/or distribution by UNFI’S customers. Extended exposure to above-refrigerated temperatures may allow growth of bacteria such as Clostridium Botulinum to reach unsafe levels, which if consumed can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled. No illnesses, including allergic reactions, involving this product have been reported to date in connection with this problem.
  Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these symptoms should seek immediate medical attention.
  A total of 75 cases of this product were distributed to 69 retail customers serviced by UNFI distribution centers in Greenwood, IN. and Sarasota, Fla. between Jan. 1, 2019 and Aug. 30, 2019 to the following states IN, KY, IL, MI, FL, OH, MO. No other distribution centers or products in states that are not listed are impacted by this notice. Additionally, Arla Apetina Marinated Feta & Olives in Oil, not sold by UNFI Greenwood or Sarasota are not impacted by UNFI’s voluntary recall.
  The product comes in a 3.1-pound plastic package marked with UPC code 9393605697.
  Retailers who have purchased the Arla Apetina Marinated Feta & Olives in Oil, Pitted product from these two distribution centers should remove any remaining product from the supply chain and discard the product in a manner that would prevent its consumption or distribution and contact their UNFI account managers for a full refund. Consumers with questions may contact the company at 800-451-2525.
• Roland Foods, LLC of New York, New York is initiating a voluntary recall of its red and black lumpfish caviar products, which were manufactured at Ora ehf in Iceland, because they have the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
  Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
  No other sizes or lots of red and black caviar or Roland® products are affected by this voluntary recall.
  No illnesses have been reported to date.
  The potential for contamination was noted after routine testing found that the product experienced a processing issue.
  Production and distribution of the product has been suspended as FDA and the company continue their investigation as to the source of the problem.
  Consumers can visit our website at http://www.rolandfoods.com
  External Link Disclaimer
  , or contact our 24-Hour Consumer Hotline at 800.221.4030 ext. 222 for further information about this voluntary recall and for further instructions.
  The Red Lumpfish Caviar and Black Lumpfish Caviar, sold in glass jars, were distributed nationwide to retailers and foodservice distributors across the United States. The UPC code is located on the back of the label, under the bar code.
• Tip Top Poultry, Inc, a Rockmart, Ga., establishment, is recalling an undetermined amount of ready-to-eat (RTE) poultry products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The frozen cooked, diced or shredded, RTE chicken products were produced between January 21, 2019 and September 24, 2019. The products subject to recall can be found in this spreadsheet. [View labels (PDF only)].
  The products subject to recall bear establishment number “Est. P-17453” inside the USDA mark of inspection. These items were shipped to institutions nationwide in the United States and Canada (see the recalled products distributed in Canada).
  The problem was discovered when the firm notified FSIS that multiple samples of product produced by Tip Top Poultry, Inc. confirmed positive for the presence of Listeria monocytogenes after being tested in Canada. The firm decided to recall all cooked, diced or shredded, RTE chicken products produced from January 21, 2019 through September 24, 2019 with product codes ranging from 10000 to 19999 and 70000 to 79999. Tip Top expanded the dates and the scope of the recall out of an abundance of caution.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
  Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
  Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
  FSIS is concerned that some product may be in institutional and consumers’ refrigerators and freezers. Consumers who have purchased these products are urged not to consume them and institutions that have purchased these products are urged not to serve them. These products should be thrown away or returned to the place of purchase.
  FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, a retail distribution list(s), if applicable, will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Consumers and media with questions regarding the recall can contact Garret Rutherford with Brand Apart, at (404) 220-9618.
• Blue Bell Ice Cream is voluntarily recalling a select lot of half gallon Butter Crunch Ice Cream produced on a specific line on August 26, 2019 in its Sylacauga, AL plant because of the possibility the products may contain a foreign object.
  Blue Bell discoveredthe issue when it was notified by a consumer of the presence of a piece of a plastic tool in a half gallon of Butter Crunch Ice Cream. The company investigation revealed the broken tool was inadvertently incorporated into the production process in a small amount of product. In an abundance of caution, the company is recalling a full day of production of this flavor from this manufacturing facility.
  The Butter Crunch Ice Cream half gallons produced in Sylacauga can be identified by the following code located on the top of the packaging lid: 082621222. An image of the affected product is included below.
  The affected Butter Crunch Ice Cream half gallons were distributed in parts of Alabama, Florida, Georgia, Kentucky, Mississippi, North Carolina, South Carolina, Tennessee, and Virginia. All affected stores are directly delivered to and serviced by Blue Bell Creameries and have been instructed to remove the product from their shelves. There have been no reports of injuries due to consumption of this product to date. This recall is being conducted in cooperation with the FDA.
  PRODUCT: Butter Crunch Ice Cream half gallons
  CODE DATE: 082621222
  Consumers who have purchased these items can return them to the place of purchase for a full refund. For more information, consumers with questions may call 979-836-7977, Monday–Friday 8 am– 5 pm CST.
•  Update – Lipari Foods has issued a voluntary recall of Premo Ham & Cheese Wedge Sandwiches and Fresh Grab Ham & Cheese Wedge Sandwiches due to potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  The product was distributed exclusively by Lipari Foods in Warren, Michigan to food service and retail stores throughout Florida, Iowa, Illinois, Indiana, Kentucky, Maryland, Michigan, Missouri, Ohio, Pennsylvania, Tennessee, West Virginia, and Wisconsin.
  The affected product can be identified by:
  Brand
  Product
  Lipari #
  Pack / Size
  Best By Date
  Lot #
  UPC
  Premo
  Wedge Ham & Cheese On Wheat
  915509
  4 / 5 oz.
  10/17/19
  24201909
  612510002001
  Fresh Grab
  Wedge Ham & Cheese On Wheat
  252646
  56 / 5 oz.
  10/17/19
  24201909
  612510002001
  Lipari Foods is expanding its recall from 10/2/19 to include one lot of Ham & Cheese Wedge Sandwiches produced by JLM Manufacturing due to potential contamination of Listeria monocytogenes. The potential for contamination of this particular lot was brought to our attention during an FDA investigation of the previous recall. No illnesses have been reported to date in relation to this recall.
  Lipari Foods began shipping this product on September 25, 2019.
  Consumers who have purchased these recalled products should not consume them. Consumers should discard the products or return them to the point of purchase. Consumers with questions should call Customer Service at 586-563-2437, 8:15 am – 4:30 pm, EST, Monday through Friday.
  Link to Original Recall
• Out of an abundance of caution, The J. M. Smucker Company today announced a voluntary recall of specific lots of Robin Hood® All Purpose Flour distributed and sold in the U.S. due to possible E. coli contamination. This recall does not impact any Robin Hood® items sold in Canada.
  No other items manufactured by The J. M. Smucker Company, including other Robin Hood® products distributed and sold in the U.S. or Canada, are impacted by this issue. No illnesses related to this issue have been reported to date.
  The impacted products are as follows:
  Product Name
  UPC Code – Case
  UPC Code – Item
  Lot Codes
  Best if Used By Dates
  Robin Hood® All Purpose Flour (5 lb)
  0 51500 18010 2
  0 51500 18010 5
  8350 513
  8351 513
  8354 513
  8355 513
  6/16/2020
  6/17/2020
  6/20/2020
  6/21/2020
  These products were distributed by The J. M. Smucker Company to a variety of retailers in the U.S.
  Consumers who have impacted product should stop using the products and should dispose of them. If consumers have questions or have products covered by this recall, they should email the Company by completing this form
  External Link Disclaimer
  or calling 888-569-6728, Monday through Friday, between 8:00 a.m. and 5:00 p.m. ET.
  The recall is being conducted in cooperation with the U.S. Food and Drug Administration.
• Premium Foods USA, Inc., a Woodside, N.Y. establishment and importer of record, is recalling approximately 121,151 pounds of various Siluriformes fish products that were not presented for import re-inspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Additionally, the products were imported from Bangladesh and Myanmar, countries ineligible to export Siluriformes fish product to the United States.
  The various Siluriformes fish items were imported from Bangladesh and Myanmar to the United States on various dates from March 20, 2018 through May 4, 2019. The spreadsheet contains a list of products subject to recall.
  These items were shipped to retail locations in Colorado, Connecticut, Florida, Georgia, Illinois, Michigan, New Jersey, New York and Pennsylvania.
  The problem was discovered during routine FSIS surveillance activities of imported products.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
  FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
• Grand Strand Sandwich is recalling Lunch Box Chicken Salad Fresh Wedges with sell by 10/29/19 to 10/08/19, Lunch Box Chicken Salad Frozen Wedges with a julian date of , Fresh and Local Chicken Salad Croissants sell by date of 10/10/19 and 9/26/19 and due to a potential contamination of Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, a Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.
  On October 3, 2019 the firm was notified by Star foods aka Mrs. Stratton’s that the chicken salad they make for Grand Strand Sandwich Company, Inc has chicken in it which is involved in a recall. Tip Top Poultry, Inc., initiated a recall and is an ingredient provider to Star Food who makes Grand Strand Sandwich Company’s Chicken Salad.
  No illnesses have been reported to date.
  Products affected are:
  Product
  Size
  UPC
  Sell By /Julian Dates
  Lunch Box Chicken Salad Fresh Wedge
  4.5 oz package
  0 67068 12105 4
  Sell by: 10/29/19 10/25/19
  10/18/19 10/15/19 10/11/19
  10/08/19
  Fresh and Local Chicken Salad Croissants
  5 oz package
  0 67068 13105 3
  Sell By
  9/19/19
  9/24/19
  9/26/19
  10/1/19
  10/3/19
  10/10/19
  Lunch Box Chicken Salad Frozen Wedge
  4.5oz package
  0 67068 12105 4
  Julian Date 26119
  The products were distributed between September 4, 2019 until October 2, 2019. These products were packaged in clear plastic and sold primarily in convenience stores and vending machines located in the States of: North Carolina and South Carolina.
  Consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Consumers with questions may contact Kirk McCumbee at 1-843-399-2999 Monday – Thursday 8AM – 4PM, Friday from 8AM – 3PM EST.
  This recall is being made with the knowledge of the Food and Drug Administration.
• Cornerstone Premium Foods of Syracuse, New York is recalling a specific lot of product containing frozen blackberries (noted below) due to the potential of being contaminated with Norovirus. FDA testing of frozen blackberries was reported to have tested positive for Norovirus.
  Norovirus is a highly contagious virus. Consumption of product contaminated with Norovirus may cause acute onset of symptoms of gastroenteritis including severe nausea, vomiting and diarrhea. Less common symptoms are low-grade fever, chills, headache, muscle aches and fatigue. Although most symptoms end within 48 hours, the elderly, young children and immunocompromised persons may develop prolonged, or more severe symptoms.
  No illnesses have been reported to date in connection with this recall. Impacted retailers have removed these products from store shelves. The FDA and the company continue to investigate the source of the issue.
  Specific lot information is as follows:
  Product
  UPC Code
  Lot Number
  Expiry Date
  Distribution Dates
  16 oz Cornerstone Frozen Blackberries
  8 55104 00765 9
  GC 1 1092 9
  April, 2021
  4/2/2019-8/7/2019
  Consumers who have purchased the products are urged to destroy or urged to return them to the place of purchase for a full refund. Consumers with questions may contact Cornerstone Premium Foods at 1-800-333-0949, Monday – Friday, 8:00AM – 5:00PM EST.
  This product was sold to various retailers in NY, MA, PA, ME, FL, AL, WI, CT, and W
• Lipari Foods has issued a voluntary recall of Lipari Old Tyme Bulk Chicken Salad, Lipari Old Tyme Bulk Cranberry Almond Chicken Salad, Premo Chicken Salad Wedge Sandwiches, Fresh Grab Chicken Salad Wedge Sandwiches, and Premo Signature Cranberry Almond Chicken Salad on Croissant due to potential contamination of Listeria monocytogenes
  Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  The product was distributed exclusively by Lipari Foods in Warren, Michigan to food service and retail stores throughout Florida, Iowa, Illinois, Indiana, Kentucky, Maryland, Michigan, Minnesota, Missouri, New York, Ohio, Pennsylvania, Tennessee, West Virginia, and Wisconsin.
  The affected product can be identified by:
  Brand
  Product
  Lipari #
  Pack / Size
  Best By Date
  UPC
  Lipari Old Tyme
  Salad Chicken
  272196
  2 / 5 lbs.
  10/2/2019 & 10/22/2019
  081466701410
  Lipari Old Tyme
  Salad Chicken Cranberry & Almonds
  656742
  2 / 5 lbs.
  10/01/2019 & 10/15/2019 & 10/22/2019
  081466703193
  Premo
  Wedge Chicken Salad On Wheat
  915530
  4 / 5 oz.
  09/19/2019 & 09/20/2019 & 09/21/2019 &
  09/22/2019 & 09/26/2019 & 09/27/2019 & 09/28/2019 & 10/13/2019 & 10/16/2019 & 10/17/2019 & 10/18/2019
  612510002032
  Premo
  *U* Wedge Chicken Salad On Wheat
  207715
  1 / 5 oz.
  09/22/2019 & 09/26/2019 & 10/16/2019
  612510002032
  Fresh Grab
  Wedge Chicken Salad On Wheat
  253377
  56 / 5 oz.
  09/19/2019 & 09/21/2019 & 09/26/2019 &
  10/17/2019
  612510002032
  Premo Signature
  Chicken Salad Cranberry Almond on
  Croissant
  915628
  4 / 5 oz.
  09/26/2019 & 09/29/2019 & 10/01/2019 &
  10/3/2019 & 10/6/2019
  612510090954
  This recall was brought to our attention by The Suter Company whose poultry supplier Tip Top Poultry has issued a voluntary recall of an undetermined amount of ready-to-eat (RTE) poultry products that may be adulterated with Listeria monocytogenes. Select dates of both Bulk Chicken Salad and Cranberry Almond Chicken Salad are being recalled at this time. Both recalled items were used by JLM Manufacturing to produce select dates of Wedge and Signature sandwiches, which are also being recalled at this time. No illnesses have been reported to date in relation to these products or recall.
  Lipari Foods began shipping this product on August 25, 2019.
  Consumers who have purchased these recalled products should not consume them. Consumers should discard the products or return them to the point of purchase. Consumers with questions should call Customer Service at 800-729-3354, 8:15 am – 4:30 pm, EST, Monday through Friday.
• E.A. Sween Company announced the recall of multiple products due to possible contamination of Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  Tip Top Poultry, Inc., initiated a recall and is an ingredient provider to two of E.A. Sween’s suppliers, The Suter Company, Inc. that provides chicken salad products and Baja Foods LLC that provides burritos, to the company. To date, we have not received any reported illnesses related to this organism.
  Retailers have been instructed to remove affected products from store shelves and inventory immediately. Customer partners with questions are asked to call our Customer Service hotline at 1-800-328-8184 and select #6 for information and refund instructions.
  Affected product could have been delivered in the Continental U.S., Hawaii and Guam through convenience stores and grocery and mass retail outlets. Consumers may return the affected product to the store where it was purchased for a full refund or exchange. If the product has been consumed, please call our Consumer Hotline, Monday through Friday from 8:00 a.m. to 4:00 p.m. CST at 1-800-328-8184 and select #5.
• Coborn’s, Inc. is recalling select chicken salad products, which may have been contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  The product recall has been initiated due to the supplier of the ready-to-eat chicken, Tip Top Poultry Inc. Rockport, GA, recalling all their chicken materials produced between January 21, 2019 and September 24, 2019.
  The recalled products were distributed and sold at Coborn’s and Cash Wise Stores in Minnesota, North Dakota and South Dakota; Marketplace Foods stores in Western Wisconsin. The table below includes the UPCs of products possibly affected.
  Product
  UPC
  How sold
  Locations Where Sold
  Cashew Chicken Salad
  207063XXXXX
  Per pound out of Deli Service Case
  All Coborn’s, Cash Wise and Marketplace Foods locations and available through online ordering at select locations
  Chicken Salad Spread
  207066XXXXX
  Per pound out of Deli Service Case
  All Coborn’s, Cash Wise and Marketplace Foods locations and available through online ordering at select locations
  Spicy Chicken Salad
  207198XXXXX
  Per pound out of Deli Service Case
  Coborn’s Delano, MN location ONLY – in store and online
  Southwest Chicken Taco Pasta
  207074XXXXX
  Per pound out of Deli Service Case
  Coborn’s Delano, MN location ONLY – in store and online
  Pulled Rotisserie Chicken Cold
  206982XXXXX
  Per random weight container
  Deli Self Service area
  Coborn’s Pinecone Road, Sartell, MN location ONLY – in store and online
  Chicken Salad Spread
  733147-10489
  12oz container
  Deli Self Service area
  All Coborn’s, Cash Wise and Marketplace Foods locations and available through online ordering at select locations
  Chicken Salad on Marble Rye
  205118XXXXX
  Each
  Deli Self Service are
  All Coborn’s, Cash Wise and Marketplace Foods locations and available through online ordering at select locations
  Chicken Salad Wrap
  206983XXXXX
  Each
  Deli Self Service are
  All Coborn’s, Cash Wise and Marketplace Foods locations and available through online ordering at select locations
  Chicken Salad Sandwich
  207209XXXXX
  Each
  Deli Self Service are
  All Coborn’s, Cash Wise and Marketplace Foods locations and available through online ordering at select locations
  Chicken Salad Croissant Sandwich
  207275XXXXX
  Each
  Deli Self Service are
  All Coborn’s, Cash Wise and Marketplace Foods locations and available through online ordering at select locations
  In an abundance of caution, Coborn’s, Inc. stores (including Cash Wise, Coborn’s and Marketplace Foods) have pulled all products that may have been affected. Any current offerings are not affected. Guests who have purchased the products listed in the table attached should destroy these products or return them to the store where they were purchased for a full refund. Guests with questions may call 1-844-414-7467 between the hours of 8:00am- 8:00 pm Monday-Friday and Saturdays and Sundays 10:00 am- 6:00 pm.
  No illnesses have been reported to date in connection with this problem. Guests with health concerns should contact a healthcare provider.
• Mical Seafood, Inc. of Cooper City, FL, voluntarily initiated a recall of frozen, wild-caught yellowfin tuna poke cubes, tuna loins, tuna ground meat and 6oz tuna steaks because of potentially elevated levels of histamine. Elevated levels of histamines can produce an allergic reaction called scombroid fish poisoning that may result in symptoms that can generally appear within minutes to several hours after eating the affected fish.
  The most common symptoms of histamine or scombroid fish poisoning are tingling or burning sensation in the mouth, facial swelling, rash, hives and itchy skin, nausea, vomiting or diarrhea; these symptoms usually resolve within several hours without medical intervention. However, each individual may experience symptoms differently. If symptoms are severe an individual should seek immediate medical attention for treatment.
  These tuna products were sold to customers in Maryland, Pennsylvania, New York, New Jersey, Florida, Texas, Alabama, North Carolina, California Michigan, Rhode Island, U.S. Virgin Islands, Sint Maarten and Grand Cayman.
  The tuna products have production dates between 04/02/2019 to 05/14/2019.
  Product Name
  Brand
  Size
  Lot Number
  Production Date
  Tuna Poke 2cm AAA IVP
  Mical Seafood
  10lb
  23910
  04/09/2019
  Tuna Poke 2cm AAA IVP
  Mical Seafood
  10lb
  24046
  04/20/2019
  Tuna Poke 2cm AAA IVP
  Mical Seafood
  10lb
  25324
  04/27/2019
  Tuna Loins 5-8lb AAA IVP
  Mical Seafood
  30lb
  20799
  04/02/2019
  Tuna Loins 5-8lb AAA IVP
  Mical Seafood
  30lb
  24037
  04/09/2019
  Tuna Loins 5-8lb AAA IVP
  Mical Seafood
  30lb
  24279
  04/24/2019
  Tuna Loins 5-8lb AAA IVP
  Mical Seafood
  30lb
  23020
  05/10/2019 Tuna Ground Meat AAA IVP
  Mical Seafood
  10lb
  25694
  05/14/2019
  Tuna Steaks 6z AA IVP
  Mical Seafood
  10lb
  23906
  04/20/2019
  Four reported illnesses have been confirmed as of 10/01/2019. While Mical Seafood feels these were isolated incidents, it has initiated this voluntary recall to take every precautionary measure when it comes to customers’ health and safety.
  Customers who received products from Lot # 23910, 24046, 25324, 20799, 24037, 24279, 23020. 25694, and 23906 with Production Dates of: 04/02/2019, 4/09/2019, 04/20/2019, 04/24/2019, 04/27/2019, 05/10/2019 and 05/14/2019 should not consume them. Inventory should be quarantined until returned to the supplier or to Mical Seafood, Inc. for a full refund.
  Customers with questions or concerns may contact the company’s Recall Team: (Jennifer Gonzalez or Margarita Alzugaray) by calling (954) 935-0133, Monday through Friday, 8 a.m. to 5 p.m., Eastern Time.
• In association with ADM Milling Company, King Arthur Flour, Inc., announced today a voluntary national recall of specific lots of its Unbleached All-Purpose Flour (5 lb. & 25 lb.)
  We are taking this voluntary precautionary step because of the potential presence of E. coli 026 which was discovered through sampling. King Arthur Flour has not received any confirmed reports of illnesses related to this product.
  This flour was milled at an ADM Milling facility in Buffalo, NY, and was distributed by King Arthur Flour through retailers and distributors nationwide, and sold through our website, catalogue, and store in Norwich, VT.
  The only product affected by this voluntary recall is our Unbleached All-Purpose Flour (5 lb. & 25 lb.) from the Best Used by Dates and Lot Codes listed below.
  King Arthur Flour Unbleached All-Purpose Flour 5 lb. UPC: 071012010509
  Best Used By:
  Lot Code
  12/04/19
  L18A04A
  12/05/19
  L18A05A, L18A05B, L18A05C
  12/09/19
  L18A09B
  12/10/19
  L18A10A
  12/13/19
  L18A13B, L18A13C
  12/20/19
  L18A20A, L18A20B, L18A20C
  12/21/19
  L18A21A
  12/27/19
  L18A27A, L18A27B, L18A27C
  12/28/19
  L18A28A
  01/02/20
  A19A02B, A19A02C
  01/03/20
  A19A03A, A19A03B, A19A03C
  01/05/20
  A19A05A, A19A05B
  01/07/20
  A19A07B, A19A07C
  01/08/20
  A19A08B
  01/09/20
  A19A09B
  01/10/20
  A19A10B
  01/12/20
  A19A12A
  01/14/20
  A19A14A, A19A14B, A19A14C
  01/15/20
  A19A15A, A19A15B
  Best Used By and Lot Code information can be found on the bottom of the ingredient side panel of the 5 lb. Bag. Best Used By date and Lot Code, along with their location on the bag, must all match in order to represent flour affected by this recall.
  King Arthur Flour Unbleached All-Purpose Flour 25 lb. UPC: 071012012503 Costco only
  Best Used By: 12/04/19, 12/10/19, 12/20/19, 01/07/20, 01/15/20
  This is an expansion of a recall announced June 13, 2019. The Lot Codes listed above join the previously voluntarily recalled Lot Codes on June 13:
  https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/association-adm-milling-co-king-arthur-flour-inc-voluntarily-recalls-limited-quantity-unbleached-all
  Consumers who have any of these affected products should throw them away and may submit a claim for a refund or replacement at kingarthurflour.com/voluntaryrecall
  External Link Disclaimer
  , or by calling our King Arthur Flour Consumer Hotline at 866-797-9178.
  Consumer safety is our top priority. Consumers are reminded to wash their hands, work surfaces, and utensils thoroughly after contact with raw dough products or flour, and to never eat raw dough or batter. The Centers for Disease Control (CDC) warns consumers to not consume raw products made with flour. E. coli O26 is killed by heat through baking, frying, sautéing, or boiling products made with flour.
  For more information, refer to the following: https://www.cdc.gov/features/no-raw-dough/index.html.
  Symptoms of E. coli O26 illness include acute, often bloody diarrheal illness and abdominal cramps. Most people recover within a week. However, children, the elderly, and immunosuppressed individuals may develop hemolytic uremic syndrome (HUS), a severe illness which may cause the kidneys to fail.
  Bakers have trusted King Arthur Flour products in their kitchens for over 225 years and because of that trust we have issued this voluntary recall. We remain committed to providing our consumers safe and superior products.
  This information can be found online at kingarthurflour.com/voluntaryrecall.
  External Link Disclaimer
  Consumers with any questions regarding this recall or King Arthur Flour products are encouraged to call the King Arthur Flour Consumer Hotline at 866-797-9178.
• Mavidon is voluntarily recalling 21 lots of LemonPrep® 4 ounce tubes and single use cups to user level. These products have been found to be contaminated with Burkholderia cepacia. The specific lots are listed below:
  Product
  Product #
  Lot#
  LemonPrep 4 oz Tubes
  MD0019-T
  29824, 29901, 30006, 30145, 30236, 30352,
  30675, 30729, 31138
  LemonPrep Single Use Cups
  MD0019-SUP
  29927, 30009, 30031, 30115, 30059, 30237,
  30300, 30340, 30424, 30642, 30735, 31139
  Burkholderia cepacia is a multi-drug resistant pathogenic microorganism. Contaminated products with Burkholderia cepacia can potentially result in serious infections, may be life-threatening for patients with compromised immune systems, such as neonates, elderly, pregnant women, cancer patients, but also in previously healthy individuals. To date, Mavidon has received one report of adverse event in a neonate related to this product in recall. Additional testing is ongoing to determine if there are other affected lots.
  The product is used as abrasive skin prepping lotion and designed to lower skin impedance and enhance the signal quality at the electrode site. This cleaning agent removes oils and skin residue on patients with normal to oily skin. The lot numbers can be identified on the LemonPrep® 4 ounce tubes can be found on the crimp and the outer box label. The single use cup lot numbers can be found on the cups and the other box label. These were distributed Worldwide to hospitals in USA, Canada, Australia, Spain, England, The Netherlands, from September 2017 to January 2019.
  Mavidon is notifying its customers by email and is arranging for the replacement of all recalled products. Hospital and clinics that have product that is being recalled should immediately stop using the product and quarantine it. Contact Mavidon at 800-654-0385 (Monday – Friday, 8:30 AM to 5:00 PM EDT) or by email to cs@mavidon.com.
  Consumers with questions regarding this recall can contact Mavidon at 800-654-0385 (Monday – Friday, 8:30 AM to 5:00 PM EDT) or by email to cs@mavidon.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to the use of this product.
  Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
• In response to a recall from Consider Bardwell Farm, Whole Foods Market stores in the Northeast and North Atlantic regions are voluntarily recalling Dorset cheese because of a potential contamination of Listeria monocytogenes.
  Listeria monocytogenesis an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, pregnant women and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages, stillbirths and fetal infection among pregnant women.
  The affected product was sold at Whole Foods Market stores in Connecticut, Maine, Massachusetts, New Hampshire, New Jersey, New York and Rhode Island. The affected product was cut and wrapped in plastic with a Whole Foods Market scale label, identifiable by PLU code 97776 with sell-by dates through 10/30/2019.
  No illnesses have been reported to date.
  Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.
• : LemonPrep Tubes and Single Use Cups by Mavidon: Recall – Due to contamination with burkholderia cepaciaAUDIENCE: Patient, Consumer, Health Professional, Risk Manager, Infectious DiseaseISSUE: Mavidon is voluntarily recalling 21 lots of LemonPrep 4 ounce tubes and single use cups to user level. These products have been found to be contaminated with burkholderia cepacia.The specific lot numbers are listed below:
  LemonPrep 4 oz Tubes
  Lot Numbers: 29824, 29901, 30006, 30145, 30236, 30352,30675, 30729, 31138LemonPrep Single Use Cups
  Lot Numbers: 29927, 30009, 30031, 30115, 30059, 30237, 30300, 30340, 30424, 30642, 30735, 31139Contaminated products with burkholderia cepacia can potentially result in serious infections, may be life-threatening for patients with compromised immune systems, such as neonates, elderly, pregnant women, cancer patients, but also in previously healthy individuals. To date, Mavidon has received one report of an adverse event in a neonate related to this product.Patients, consumers and health professionals are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:
• Consider Bardwell Farm, LLC of West Pawlet, Vermont, is recalling the following cheeses:
  Product Name
  Unit Size
  Comments
  Product Code
  Product Dates
  Slyboro
  2 pound wheel
  Units per case: 2
  Case dimensions: 12”x 6”x 4”
  Gross case weight: 4 lb
  Pallet boxes per layer (TI): 24
  Pallet number of tiers (HI): 12
  Cases per pallet: 288
  All in your possession
  4/28/2019 until present
  Dorset
  2.5 pound wheel
  Units per case: 4
  Case dimensions: 8”x 8”x10”
  Gross case weight: 10 lb
  Pallet boxes per layer (TI): 30
  Pallet number of tiers (HI): 8
  Cases per pallet: 240
  All in your possession
  4/28/2019 until present
  Experience
  Three quarters pound square
  Units per case: 8
  Case dimensions: 12”x 6”x 4”
  Gross case weight: 4 lb
  Pallet boxes per layer (TI): 24
  Pallet number of tiers (HI): 12
  Cases per pallet: 288
  All in your possession
  4/28/2019 until present
  These products have been distributed in: CA, MA, NY, TX, VT.
  These products may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant women.
  No illnesses have been reported to date in connection with these products. This is a voluntary and precautionary recall initiated by Consider Bardwell Farm. The contamination was discovered by routine testing of finished products and the manufacturing environment.
  Consumers who have purchased products listed in the above table are urged to return these products to the place of purchase for a full refund. Consumers with questions may contact the company at 802-645-9928
• Port Jefferson Station, NY, Cellect Products Inc. and Oglethorpe Ltd. are voluntarily recalling lot #041907 of Cellect Unflavored Powder & Essentials Factor Cell Synergy Unflavored Powder (1.25 LB) to the retail and consumer level. The Cellect Unflavored Powder & Essentials Factor Cell Synergy Unflavored Powder has been found to have unsafe levels of Arsenic and Lead.
  Risk Statement: “Long-term exposure to inorganic arsenic has been associated with skin disorders and increased risks for skin, bladder, and lung cancers’
  Taking more than two (2) servings daily potentially could result in an accumulation of Lead in the body over time and too much of it can cause serious and sometimes permanent adverse health consequences. People with high blood levels of lead may show no symptoms, but the condition may cause damage to the nervous system and internal organs. Acute lead poisoning may cause a wide range of symptoms, including abdominal pain, muscle weakness, nausea, vomiting, diarrhea, weight loss, and bloody or decreased urinary output. Children are particularly vulnerable to lead poisoning. Lead poisoning can be diagnosed through clinical testing.
  Cellect Products Inc. and Oglethorpe Ltd. have not received any reports of adverse events related to this recall to date.
  The product is used as a supplement and is packaged in a white plastic bottle.The affected Cellect Unflavored Powder & Essentials Factor Cell Synergy Unflavored Powder has the following lot #041907 and a manufactured (MFG) date of 05/20/2019 stamped on the bottom. The product can be identified as a Multi-Mineral & Vitamin Supplement. The Cellect Unflavored Powder & the Essentials Factor Cell Synergy Unflavored Powder are distributed via retail and the internet to the USA and to individual customers in Canada, United Kingdom, Netherlands, Switzerland, France, Croatia, Romania, Russia, Australia, New Zealand, South Korea, Singapore, China, India, Thailand, and Japan.
  Cellect Products Inc. and Oglethorpe Ltd. are notifying its distributors and customers by email or mail and are arranging for the return and replacement of all recalled products. Consumers, distributors and retailers that have Cellect Unflavored Powder or Essentials Factor Cell Synergy Unflavored Powder which is being recalled should stop using and return to place of purchase for a replacement or a refund.
  Consumers with questions regarding this recall can contact Cellect Products Inc. and Oglethorpe Ltd. by phone at 631-509-5316, Monday-Friday 11am-5pm Eastern Time or send an e-mail to request@cellect.org. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
  This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

The agency was formally established by Truman in a memorandum of October 24, 1952, that revised National Security Council Intelligence Directive (NSCID) 9. Since President Truman’s memo was a classified document, the existence of the NSA was not known to the public at that time.