Diary of Anne Frank opens at the Music Box Theater in New York City. by sabrina-lee

The Diary of Anne Frank is the stage adaptation of the book The Diary of a Young Girl. It opened on October 5, 1955, at the Cort Theater, Broadway, and ran until 1957. It received several awards, such as the Tony Award for Best Play, the New York Drama Critics Circle award for Best Play, the Pulitzer Prize for Drama, and more.

On this day, December 4, in 1977, the revived version of the play opened at the Music Box Theater.

Twenty years later the play was revived again as George Hearn played the part of Otto Frank and Natalie Portman took on the role of Anne. The production received two Tony Award nominations in 1999 for Best Revival of a Play and for Best Featured Actress as well as two Drama Desk nominations for Outstanding Featured Actor and Actress.

Resources: famousdaily.com   playbill.com

Image by viator

There may be or look like duplicate reports from companies or fda recalls … in some instances …yes, others are updates or additional information

• UNFI announced today a voluntary national recall of five-pound bags of its Wild Harvest® Organic All-Purpose Flour, Unbleached, with a Code of AA BEST IF USED BY 010820 CC 15:58 and UPC Code 711535509158. The recall is being issued for the potential presence of E. coli. During routine FDA sampling of the five-pound bag product, results were found to be positive for E.coli.
  E. coli can cause serious and sometimes life-threatening infections in infants, older people, pregnant women, and people with weakened immune systems. The most common symptoms of E. coli are diarrhea, abdominal cramps, nausea and vomiting, which develop within three or four days of eating contaminated food. The illness usually lasts about a week and most people recover without treatment. Guidance from FDA and the Centers for Disease Control (CDC) continues to warn that consumers should refrain from consuming any raw products made with flour and that all surfaces, hands and utensils should be properly cleaned after contact with flour or dough.
  To date, UNFI has not received any direct consumer reports of confirmed illnesses related to this product. This recall is being issued out of an abundance of care.
  This recall only affects the following code date of Wild Harvest® Organic All-Purpose Flour, Unbleached five-pound bags currently in stores or consumers’ pantries. No other types of Wild Harvest® Flour are affected by this recall.
  Wild Harvest® Organic All-Purpose Flour, Unbleached (sample label below) Package UPC: 711535509158 Best if Used by Date: 010820 CC 15:58 (can be found on top of the product, see sample below)
  Consumers are asked to check their pantries and dispose of the product affected by this recall. Consumers with questions may contact UNFI at 855-423-2630 (customer support is available seven days-a-week between 8:00 AM to 8:00 PM CST). Any consumers concerned about an illness should contact a physician.
• Hodgson Mill of Effingham, IL, announced today a voluntary national recall of specific lots of its Unbleached All-Purpose White Wheat Flour (5 lb.)
  We are taking this voluntary precautionary step because of the potential presence of pathogenic E. coli which was discovered through sampling raw uncooked flour. Hodgson Mill has not received any confirmed reports of illnesses related to this product.
  The only product affected by this voluntary recall is:
  Unbleached All-Purpose White Wheat Flour (5 lb.) UPC 0-71518-05009-2
  Best By Date 10-01-2020 and 10-02-2020 with lot codes listed Lot# 001042 & 005517
  Use By and Lot Code information can be found on the bottom back panel of the 5 lb. Bag. 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.
  Consumer safety is our top priority. Hodgson Mill package states “do not eat raw flour, dough or batter”. The Centers for Disease Control (CDC) warns consumers to not consume raw flour or uncooked raw dough.
  E. coli 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 pathogenic E. coli 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.
  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.
  This lot of flour was milled at an ADM Milling Facility in St Louis, MO and repacked at Hodgson Mill, Inc. facility in Effingham, IL and was distributed by Hodgson Mill through retailers and distribution nationwide and sold through our website http://www.hodgsonmill.com
  External Link Disclaimer
  .
  Consumers who have purchased 5 lb packages of Unbleached All-Purpose White Wheat Flour with specific lot codes are urged to stop using the product immediately and return them to the place of purchase for a full refund. Consumers with questions may contact the company customer service M-F 9am to 3pm at 1-888-417-9343 x 1.
• Whole Foods Market is voluntarily recalling one lot code of Whole Foods Market Raspberry Cheesecake Italian Gelato because these product units contain egg that is not listed on the product label. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume the product.
  The affected product was sold at Whole Foods Market stores nationwide. The product was packaged in 1-pint plastic containers with the UPC 9948248024 and a best by date of 6/11/2021. The issue was discovered after the grocer determined that some Butter Cookies and Sweet Cream Italian Gelato were mistakenly packed by its supplier in containers labeled for Raspberry Cheesecake Italian Gelato. All affected product has been removed from store shelves. No reactions 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. CST Saturday through Sunday.
• Northern Fisheries LTD of Little Compton, RI, has expanded their voluntary recall of frozen, wild-caught yellowfin Tuna Medallions (product of Vietnam) to include product sold directly to consumers. This recall is 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 sold to customers in: CT, MI, MN, RI and WI.
  ALL LOTS WITH PRODUCTION DATE: 06/13/2019 UPC Code: 815838020638
  Production date and UPC Code can be found on back of the Tuna King Brand rider card.BRAND
  DESCRIPTION
  PRODUCTION DATE:
  NORTHERN
  LOT #
  UPC CODE
  Tuna King
  Tuna Medallions 2-3oz 10x1lb
  06/13/2019
  0058797
  815838020638
  Customers who received products with the listed Production Date of: 06/13/2019 should not consume them and should discard them immediately.
  Customers with questions or concerns may contact Northern Fisheries LTD by calling (401) 592-0600, Monday through Friday, 9 a.m. to 5 p.m., Eastern Time or email.
  northfish@northfishltd.com
• Vitamin Cottage Natural Food Markets, Inc., a Lakewood, Colorado-based natural grocery chain, is recalling Natural Grocers brand 2-pound Organic Soybeans because they have the potential to contain mold. Consumers who may have purchased this product are advised to discontinue use and either throw it away or return it to the store for credit or refund.
  The recalled product is packaged in clear plastic bags weighing 2 pounds and bearing the “Natural Grocers” label. Only packages bearing 19-168 and 19-205 as the packed-on dates are subject to recall. The packed-on date can be found in the bottom left-hand corner of the label.
  The potential for contamination was noted after routine testing by the company revealed the presence of mold.
  Production of the product has been suspended while the Food and Drug Administration and the company continue their investigation into the source of the problem.
  UPC Code
  Description
  Packed on Dates
  000080663607
  Organic Soybeans 2 LB
  19-168 & 19-205
  The product was distributed to 154 Natural Grocers’ stores located in Arkansas, Arizona, Colorado, Iowa, Idaho, Kansas, Louisiana, Minnesota, Missouri, Montana, Nebraska, Nevada, New Mexico, North Dakota, Oklahoma, Oregon, Texas, Utah, Washington and Wyoming. Consumers can find the specific locations of Natural Grocers’ stores in those states at: https://www.naturalgrocers.com/store-directory
  External Link DisclaimerDisclaimer
  Consumers with questions may contact the company by calling Customer Service at 303-986-4600, ext. 80801, Monday through Friday 8:00 a.m. to 5:00 p.m. (MST).
• Amneal Pharmaceuticals, LLC. Bridgewater, New Jersey is voluntarily recalling Ranitidine Tablets, 150 mg and 300 mg, and Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL to the consumer level. A listing of the recalled lots is identified below.
  Ranitidine Tablets, USP, 150 mg and 300 mg, and Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL, are being recalled because of potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.
  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.
  Amneal Pharmaceuticals, LLC. has not received any reports of adverse events that have been confirmed to be directly related to this recall. Ranitidine Tablets, USP and Ranitidine Syrup (Ranitidine Oral Solution, USP), manufactured by Amneal, are prescription oral products. Ranitidine is a histamine-2 blocker, which decreases the amount of acid created by the stomach. Prescription ranitidine is approved for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.
  The Ranitidine Tablets, USP and Ranitidine Syrup (Ranitidine Oral Solution, USP) subject to the recall can be identified by NDC numbers stated on the product label:
  Product
  Strength
  Pack Size
  NDC Number
  Ranitidine Tablets, USP
  150 mg
  60 count
  65162-253-06
  Ranitidine Tablets, USP
  150 mg
  100 count
  65162-253-10
  Ranitidine Tablets, USP
  150 mg
  180 count
  65162-253-18
  Ranitidine Tablets, USP
  150 mg
  500 count
  65162-253-50
  Ranitidine Tablets, USP
  150 mg
  1000 count
  65162-253-11
  Ranitidine Tablets, USP
  150 mg
  1000 count
  53746-253-10
  Ranitidine Tablets, USP
  300 mg
  30 count
  65162-254-03
  Ranitidine Tablets, USP
  300 mg
  100 count
  65162-254-10
  Ranitidine Tablets, USP
  300 mg
  250 count
  65162-254-25
  Ranitidine Tablets, USP
  300 mg
  250 count
  53746-254-02
  Ranitidine Syrup (Ranitidine Oral Solution, USP)
  15 mg/mL;
  6 fl. oz.
  473 mL
  65162-664-90
  The affected Ranitidine Tablets, USP and Ranitidine Syrup (Ranitidine Oral Solution, USP) were distributed directly to Wholesalers, Distributors, Retailers and Repackagers.
  Amneal is notifying its direct customers via mail (UPS Standard Overnight) by mailing a recall notification letter and is arranging for return of all recalled product. Anyone with an existing inventory of the product should quarantine the recalled lots immediately.
  Customers who purchased the impacted product directly from Amneal can call Stericycle at 866-918-8768, Monday – Friday, 8:00 am – 5:00 pm, EST to arrange for product return.
  Consumers who have Ranitidine Tablets, USP and Ranitidine Syrup (Ranitidine Oral Solution, USP) which are being recalled should stop using the product and can call Stericycle at 866-918-8768, Monday – Friday, 8:00 am – 5:00 pm, EST for further information.
  Consumers who would like to report adverse reactions or quality problems experienced with the use of this product can contact Amneal Drug Safety by phone at 1-877-835-5472, Monday thru Friday, 8:00 am – 6:00 pm, EST, or e-mail at DrugSafety@amneal.com.
  Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to the use of 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
  The following lot numbers of Ranitidine Tablets, USP, 150 mg & 300 mg and Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL are included in this recall.
  Ranitidine Tablets, USP, 150mg
  NDC No.
  Description
  Lot
  Expiration Date
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HB03718A
  3/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HB03818A
  3/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HB03918A
  3/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HB04018A
  3/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HC01618A
  3/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HC14618A
  5/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HC14718A
  5/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HC14818A
  5/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HC14918A
  5/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HC15018A
  5/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HK02318A
  9/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HK02418A
  9/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HK02518A
  9/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HK02618A
  9/2020
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HD03119A
  3/2021
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HD03219A
  3/2021
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HE03119A
  4/2021
  53746-253-10
  Ranitidine Tablets, USP 150mg
  HE03219A
  4/2021NDC No.
  Description
  Lot
  Expiration Date
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR171764A
  11/2019
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR171875A
  11/2019
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR171876A
  11/2019
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR171981A
  11/2019
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180020C
  1/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180206A
  1/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180207A
  1/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180208A
  1/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180438A
  2/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180439A
  2/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180481A
  3/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180482A
  3/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR180483A
  3/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR181690A
  10/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR181691A
  10/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR181806A
  11/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR190058A
  12/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR190059A
  12/2020
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR190183A
  1/2021
  65162-253-06
  Ranitidine Tablets, USP 150mg
  AR190184A
  1/2021NDC No.
  Description
  Lot
  Expiration Date
  65162-253-10
  Ranitidine Tablets, USP 150mg
  AR171984A
  12/2019
  65162-253-10
  Ranitidine Tablets, USP 150mg
  AR180020B
  1/2020
  65162-253-10
  Ranitidine Tablets, USP 150mg
  AR180675A
  4/2020
  65162-253-10
  Ranitidine Tablets, USP 150mg
  AR180868B
  5/2020
  65162-253-10
  Ranitidine Tablets, USP 150mg
  AR181807A
  11/2020
  65162-253-10
  Ranitidine Tablets, USP 150mg
  AR190366B
  2/2021NDC No.
  Description
  Lot
  Expiration Date
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR171986A
  12/2019
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR171987A
  12/2019
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180255A
  1/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180441A
  2/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180442A
  2/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180559A
  3/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180560A
  3/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180594A
  3/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180595A
  3/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180829A
  4/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180831A
  5/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180832A
  5/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR180868A
  5/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR181807C
  11/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR190085A
  12/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR190086A
  12/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR190087A
  12/2020
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR190124A
  1/2021
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR190542B
  3/2021
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR190609A
  3/2021
  65162-253-11
  Ranitidine Tablets, USP 150mg
  AR190610A
  3/2021NDC No.
  Description
  Lot
  Expiration Date
  65162-253-18
  Ranitidine Tablets, USP 150mg
  AR171875B
  11/2019
  65162-253-18
  Ranitidine Tablets, USP 150mg
  AR180483B
  3/2020
  65162-253-18
  Ranitidine Tablets, USP 150mg
  AR181807B
  11/2020
  65162-253-18
  Ranitidine Tablets, USP 150mg
  AR190008B
  12/2020NDC No.
  Description
  Lot
  Expiration Date
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171763A
  11/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171764B
  11/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171874A
  11/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171875C
  11/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171877B
  11/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171878B
  11/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171982A
  11/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171983A
  12/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR171985A
  12/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180016A
  12/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180017A
  12/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180018A
  12/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180019A
  12/2019
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180020A
  1/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180208B
  1/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180256A
  1/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180291A
  1/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180292A
  1/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180293A
  1/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180294A
  2/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180295A
  2/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180364A
  2/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180365A
  2/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180366A
  2/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180367A
  2/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180368A
  2/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180440B
  2/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180484A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180485A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180556A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180557A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180558A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180596A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180597A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180598A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180599A
  3/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180675B
  4/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180676A
  4/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180677A
  4/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180678A
  4/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180679A
  4/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180801A
  4/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180802A
  4/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180803A
  4/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180869A
  5/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180870A
  5/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180871A
  5/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180872A
  5/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180994A
  5/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180995A
  5/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180996A
  5/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180997A
  6/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR180998A
  6/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181158A
  7/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181159A
  7/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181160A
  7/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181161A
  7/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181692A
  10/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181693A
  10/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181694A
  10/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181709A
  10/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181710A
  11/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181711A
  11/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181808A
  11/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR181809A
  11/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190004A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190005A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190006A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190007A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190008A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190088A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190089A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190090A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190121A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190122A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190123A
  12/2020
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190125B
  1/2021
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190181A
  1/2021
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190182A
  1/2021
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190364A
  2/2021
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190365A
  2/2021
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190366A
  2/2021
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190509A
  3/2021
  65162-253-50
  Ranitidine Tablets, USP 150mg
  AR190510A
  3/2021Ranitidine Tablets, USP, 300mg
  NDC No.
  Description
  Lot
  Expiration Date
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB04118A
  2/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB04218A
  2/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB04318A
  2/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB04418A
  2/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HF13518A
  6/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HF13618A
  6/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HF13718A
  6/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HF13818A
  6/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HK02818A
  9/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HK02918A
  9/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HK03018A
  9/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HK03118A
  9/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HL08418A
  11/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HL08518A
  11/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HL08618A
  11/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HL08718A
  11/2020
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB01419A
  1/2021
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB05619A
  1/2021
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB05719A
  1/2021
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB05819A
  1/2021
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB05919A
  1/2021
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB06019A
  1/2021
  53746-254-02
  Ranitidine Tablets, USP 300mg
  HB06119A
  1/2021

  NDC No.
  Description
  Lot
  Expiration Date
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR172033B
  11/2019
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR180024A
  12/2019
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR180025A
  12/2019
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR180118A
  12/2019
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR180119A
  12/2019
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR180519A
  3/2020
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR180615A
  3/2020
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR181795A
  11/2020
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR181921B
  12/2020
  65162-254-03
  Ranitidine Tablets, USP 300mg
  AR190705A
  4/2021

  NDC No.
  Description
  Lot
  Expiration Date
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR172029A
  11/2019
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR172030A
  11/2019
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180021A
  12/2019
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180022A
  12/2019
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180023A
  12/2019
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180123A
  12/2019
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180144A
  1/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180145A
  1/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180146A
  1/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180147A
  1/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180402A
  2/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180465A
  2/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180466A
  2/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180467A
  2/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180468A
  2/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR180613A
  3/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR181156A
  7/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR181157A
  7/2020
  65162-254-10
  Ranitidine Tablets, USP 300mg
  AR190418B
  2/2021

  NDC No.
  Description
  Lot
  Expiration Date
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171800A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171801A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171802A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171803A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171804A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171931A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171932A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171933A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171934A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171935A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171936A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR171937A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR172026A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR172027A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR172028A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR172031A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR172032A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR172033A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR172034A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR172035A
  11/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180030A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180031A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180032A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180033A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180034A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180113A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180114A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180115A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180117A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180120A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180121A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180122A
  12/2019
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180148A
  1/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180198A
  1/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180199A
  1/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180200A
  1/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180201A
  1/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180202A
  1/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180257A
  1/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180258A
  1/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180335A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180336A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180337A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180338A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180339A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180374A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180375A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180376B
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180403A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180404A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180405A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180406A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180424A
  2/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180486A
  3/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180487A
  3/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180488A
  3/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180515A
  3/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180516A
  3/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180517A
  3/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180518A
  3/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180638A
  3/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180640A
  4/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR180641A
  4/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR181920A
  12/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR181921A
  12/2020
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR190414B
  2/2021
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR190415A
  2/2021
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR190416A
  2/2021
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR190417A
  2/2021
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR190418A
  2/2021
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR190543A
  3/2021
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR190544A
  3/2021
  65162-254-25
  Ranitidine Tablets, USP 300mg
  AR190545A
  3/2021
  Ranitidine Syrup (Ranitidine Oral Solution, USP)
  NDC No.
  Description
  Lot
  Expiration Date
  65162-664-90
  Ranitidine Syrup 15mg/mL
  06648001A
  11/2019
  65162-664-90
  Ranitidine Syrup 15mg/mL
  06648003A
  4/2020
  65162-664-90
  Ranitidine Syrup 15mg/mL
  06649001A
  1/2021

  This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
  Safe Harbor Statement

• Northern Fisheries LTD of Little Compton, RI, has expanded their voluntary recall of frozen, wild-caught yellowfin Tuna Medallions (product of Vietnam) to include product sold directly to consumers. This recall is 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 sold to customers in: CT, MI, MN, RI and WI.
  ALL LOTS WITH PRODUCTION DATE: 06/13/2019 UPC Code: 815838020638
  Production date and UPC Code can be found on back of the Tuna King Brand rider card.BRAND
  DESCRIPTION
  PRODUCTION DATE:
  NORTHERN
  LOT #
  UPC CODE
  Tuna King
  Tuna Medallions 2-3oz 10x1lb
  06/13/2019
  0058797
  815838020638
  Customers who received products with the listed Production Date of: 06/13/2019 should not consume them and should discard them immediately.
  Customers with questions or concerns may contact Northern Fisheries LTD by calling (401) 592-0600, Monday through Friday, 9 a.m. to 5 p.m., Eastern Time or email.
• “Euroline Foods LLC” of Staten Island, NY is recalling its 17.65oz (500 gram) packages of “DRY FRUIT MIX “QUINCE COMPOTE” ” because they contain undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.The recalled “DRY FRUIT MIX “QUINCE COMPOTE” were distributed nationwide in retail stores and through mail orders. The product comes in 17.65oz (500 gram), clear plastic package marked with container code# 27032019. Product UPC code is 4605932006203.No illness or allergic reactions involving this product have been reported to date.The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the 17.65oz (500 gram) packages of “DRY FRUIT MIX “QUINCE COMPOTE”“ which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reaction in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites. Analysis of the “DRY FRUIT MIX “QUINCE COMPOTE” ” revealed they contained 31.7 mg per serving.
• Ajinomoto Foods North America, Inc., an Oakland, Miss. establishment, is recalling approximately 172,692 pounds of chicken fried rice products that may be contaminated with extraneous materials, specifically pieces of plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The not-ready-to-eat, frozen chicken fried rice items were produced from July 9, 2019 to July 11, 2019 with various packaging and best by dates. The following products are subject to recall: [View Labels (PDF only)]
  54-oz. cardboard packages containing “AJINOMOTO YAKITORI CHICKEN WITH JAPANESE-STYLE FRIED RICE” with date codes “3559007, 3559008, 3559015, 3559190 and 3559191” and best by dates of “1/7/2020, 1/8/2020, 1/15/2020, 7/9/2020 and 7/10/2020.”
  The products subject to recall bear establishment number “P-34708” inside the USDA mark of inspection. These items were shipped to retail locations in Florida, Georgia, Illinois, Maryland, Michigan, New Jersey and Texas.
  The problem was discovered after the firm received consumer complaints. The firm then notified FSIS of the issue.
  There have been no confirmed reports of adverse reactions due to consumption of these products. FSIS has received no additional reports of injury or illness from 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 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.
  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.
  Consumers with questions about the recalls can contact Willis Hwang, Consumer Affairs Manager, Ajinomoto Foods North America, Inc., at (503) 361-5003 or at Willis.Hwang@ajinomotofoods.com. Members of the media with questions about the recall can contact Paul Taylor, Vice President, Ajinomoto Foods North America, Inc., at (909) 477-4800 or at TaylorP@ajiusa.com.
• Central Valley Meat Co., Inc., a Hanford, Calif. establishment, is recalling approximately 34,222 pounds of ground beef products that may be contaminated with Salmonella Dublin, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The ground beef items were produced on July 23, 2019. The following products are subject to recall: [View Labels (PDF only)]
  1-lb. chub packages of “STATER BROS. 100% PURE GROUND BEEF 96% LEAN 4% FAT” with lot 2049 on the retail label; lot 19204 on the case label; and Use By 08-14-19.
  2-lb. chub packages of “STATER BROS. 100% PURE GROUND BEEF 93% LEAN 7% FAT” with lot 2049 on the retail label; lot 19204 on the case label; and Use By 08-14-19.
  20-lb. cases containing “STATER BROS 93/7 Ground Beef 10# Chub 10 Lb. Chubs/ 2 Count” with lot 19204 on the case label and Use By 08-14-19.
  The products subject to recall bear establishment number “EST. 6063A” printed on the retail labels next to the lot number and inside the USDA mark of inspection on the case labels. These items were shipped to retail locations in California.
  FSIS was notified of an investigation of Salmonella Dublin illnesses on September 9, 2019. Working in conjunction with the Centers for Disease Control and Prevention (CDC), and state and local public health partners, FSIS determined that there is a link between ground beef products from Central Valley Meat Co., Inc., and this illness cluster. The traceback investigation indicated that a case-patient consumed ground beef produced by Central Valley Meat Co., Inc. Based on epidemiological investigation, 10 case-patients have been identified in 6 states with illness onset dates ranging from August 8, 2019 to September 22, 2019. Additional information may be found on the CDC website at https://www.cdc.gov/salmonella/dublin-11-19/index.html. This outbreak strain of Salmonella Dublin did not identify any antibiotic resistance. FSIS continues to work with the CDC and state and local public health partners on this investigation and will provide updated information as it becomes available.
  Consumption of 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 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.
  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.
  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.
  Media and consumers with questions regarding the recall can contact Josh Bornemann, CFO for Central Valley Meat Co., Inc., at inquiry@centralvalleymeat.com.
• Mondelēz Global LLC announced today a voluntary recall of a limited quantity of Cheese Nips (11 oz. Box) product in the United States due to the potential presence of small food-grade yellow plastic pieces from a dough scraper that was incorporated into the production process of a small amount of product. The company became aware of this issue when yellow plastic pieces were noticed on the manufacturing equipment.
  This recall is limited exclusively to the Cheese Nips product listed in the grid, available at retail stores nationwide. No other Mondelēz Global LLC products nor any other geographies are included in or affected by this recall.
  Description
  Retail UPC
  Best When Used By Date
  CHEESE NIPS (11 oz. BOX)
  0 44000 03453 5
  18MAY20
  19MAY20
  20MAY20
  There have been no reports of injury or illness reported to Mondelēz Global to date related to this product.
  Consumers who have this product should not eat it, and should discard any product they may have. Consumers can contact the company at 1-844-366-1171, 24 hours a day to get more information about the recall, and Consumer Relations specialists are available Monday- Friday, 9am to 6pm EST.
• Missa Bay, LLC, a Swedesboro, N.J. establishment, is recalling approximately 75,233 pounds of salad products that contain meat or poultry because the lettuce ingredient may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The salad products items were produced from October 14, 2019 through October 16, 2019. The products subject to the recall can be found on the following spreadsheet. [View Labels (PDF only)]
  The products subject to recall bear establishment number “EST. 18502B” inside the USDA mark of inspection. These items were shipped to distribution locations in Alabama, Connecticut, Florida, Georgia, Illinois, Indiana, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Virginia and Wisconsin.
  As part of a foodborne illness outbreak investigation, the Maryland Department of Health collected an unopened package of Ready Pac Bistro Chicken Raised Without Antibiotics Caesar Salad with FSIS EST number 18502B on the label. The state collected and tested individual ingredients in the salad and the lettuce tested positive for E. coli O157:H7. All products from the same lot of lettuce are included in the recall.
  Most people infected with STEC O157:H7 develop diarrhea (often bloody) and vomiting. Some illnesses last longer and can be more severe. Infection is usually diagnosed by testing of a stool sample. Vigorous rehydration and other supportive care is the usual treatment; antibiotic treatment is generally not recommended. Most people recover within a week, but, rarely, some develop a more severe infection. Hemolytic uremic syndrome (HUS), a type of kidney failure, is uncommon with STEC O157:H7 infection. HUS can occur in people of any age but is most common in children under 5 years old, older adults and persons with weakened immune systems. 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 products may be in consumers’ refrigerators even though they are past their use by dates. 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 with questions regarding the recall can contact Mary Toscano, Consumer Affairs Manager for Bonduelle at 1-800-800-7822. Members of the media with questions regarding the recall can contact the Bonduelle Newsroom at (626) 678-2222 or bfa-newsroom@bonduelle.com.
• Precision Dose Inc. is voluntarily recalling 5 lots of Ranitidine Oral Solution, USP 150 mg/10 mL to the consumer level. Ranitidine Oral Solution, USP 150 mg/10 mL, is being recalled because of potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA. This recall is being initiated in response to the recall by the manufacturer (Amneal Pharmaceuticals. LLC), which included lots that were repackaged by Precision Dose Inc.
  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. Precision Dose Inc. has not received any reports of adverse events related to this recall to date.
  Ranitidine is a histamine-2 blocker, which decreases the amount of acid created by the stomach. Prescription Ranitidine is approved for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.
  Ranitidine Oral Solution, USP 150 mg/10 mL is packaged in unit dose cups (NDC 68094-204-59) and sold in 30-pack cartons (68094-204-62) or 100-pack cartons (68094–204-61). The affected Ranitidine Oral Solution, USP 150 mg/10 mL lots are:Lot
  Expiry
  501290
  30-Nov-2019
  501326
  30-Nov-2019
  501501
  30-Nov-2019
  501592
  30-Apr-2020
  501679
  30-Apr-2020
  The lot number and expiration date are printed on each unit dose cup and carton label. Ranitidine Oral Solution, USP 150 mg/10 mL was distributed Nationwide to Wholesalers, Distributors and Hospitals.
  Precision Dose Inc. is notifying its distributors and direct customers by certified mail and is arranging for return of all recalled products. Customers, who purchased the impacted product directly from Precision Dose Inc., can call us at 815-624-8523, Monday – Friday, 8:00 am – 4:30 pm, CST to arrange for product return. Consumers, distributors and retailers that have Ranitidine Oral Solution, USP 150 mg/10 mL, which is being recalled, should stop using and call Precision Dose Inc. at 815-624-8523 to obtain a return packet.
  Consumers with questions regarding this recall can contact Precision Dose Inc. by phone (815-624-8523), Monday through Friday 8 am to 4:30 pm CST or e-mail us at: druginfo@precisiondose.com.
  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.
• The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to illnesses caused by E. coli O157:H7 associated with romaine lettuce from the Salinas, California, growing region. FSIS warns against consuming any wraps, sandwiches, prepackaged salad, salad kits, or other product containing romaine lettuce harvested from the Salinas, California, growing region. Additionally, consumers should not eat any salad products identified in a Missa Bay, LLC, recall announced by FSIS on November 21, 2019.
  On November 22, 2019, the Centers for Disease Control and Prevention (CDC) and Food and Drug Administration (FDA) advised consumers, retailers, and restaurants not to eat or sell any romaine lettuce harvested from the Salinas, California, growing region. Most romaine lettuce products at retail are labeled with a harvest location showing where they were grown. CDC and the FDA are advising that if this voluntary label indicates that the romaine lettuce was grown in “Salinas” (whether alone or with the name of another location) do not eat it. If the romaine does not have information about harvest region or does not indicate that it has been grown indoors (i.e. hydroponically- and greenhouse-grown), throw it away or return it to the place of purchase.
  FSIS-regulated establishments are advised not to serve, ship, or sell products that contain romaine lettuce from the Salinas, California, growing region. This advice includes all types of romaine lettuce from the Salinas, California, growing region, such as whole heads of romaine, hearts of romaine, and packages of precut lettuce and salad mixes that contain romaine, including baby romaine, spring mix, and Caesar salad. If you do not know the source of your romaine lettuce, and if you cannot obtain that information from your supplier, you should not serve, ship, or sell the product.
• Select varieties of Breakstone’s Cottage Cheese are voluntarily being recalled due to the potential presence of pieces of red plastic and metal that may have been introduced during production. Consumption of hard or sharp foreign material could cause injury to teeth, mouth, throat, stomach or intestine tissues if swallowed.
  The company discovered the issue when it was notified by a consumer of the presence of a piece of red plastic in a container of cottage cheese. There have been six consumer complaints and no reports of illness or injury related to this issue to date.Product Size
  Name of Product
  Packaging Description
  Case Unit Best When Used By Code Date
  Individual Package Best When Used By Code Date
  Individual Package UPC
  16oz
  Breakstone’s 2% Milkfat Lowfat Large Curd Cottage Cheese
  Plastic Cup, Plastic Lid, Shrink Band
  Dec102019
  10 DEC 2019 W4 XX:XX 36-2158
  0 21000 30053 2
  24oz
  Breakstone’s 4% Milkfat Large Curd Cottage Cheese
  Plastic Cup, Plastic Lid, Shrink Band
  Dec102019
  10 DEC 2019 W4 XX:XX 36-2158
  0 21000 12285 1
  24oz
  Breakstone’s 4% Milkfat Small Curd Cottage Cheese
  Plastic Cup, Plastic Lid, Shrink Band
  Dec102019
  10 DEC 2019 W4 XX:XX 36-2158
  0 21000 12284 4
  Approximately 9,500 cases of Breakstone’s Cottage Cheese is being recalled. No other sizes, varieties or code dates are included in this recall.
  We deeply regret this situation and apologize to any consumers we have disappointed.
  Consumers who purchased this product should not eat it and return it to the store where purchased for an exchange or full refund. Consumers with questions may contact the company at 1-866-572-3805 Monday through Friday, 9 a.m. to 6 p.m. Eastern, for a full refund.
  This product was sent to retailers and distributors in the U.S and exported to Latin America and was produced and distributed by Kraft Heinz Foods Company.
• • 113-2019, Central Valley Meat Co., Inc. Recalls Ground Beef Products Due to Possible Salmonella Dublin Contamination(Nov 15, 2019)
• Russ Davis Wholesale (RDW), a leading fresh produce processor and distributor, in an abundance of caution is voluntarily recalling 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.
  This recall is in response to Mann Packaging, Inc. initiating a recall late in the day November 3, 2019 as an ingredient provider to Russ Davis Wholesale.
  To date, Russ Davis Wholesale has not received any reported illnesses related to this organism.
  The affected products are:
  UPC
  Product Name:
  Retail Items
  Brand Name on Label
  Packaging
  SELL BY Date
  795631808148
  Broccoli, Cauliflower & Carrots with Butter – 18 oz
  Small Generic clear label on Q & E Steamer bag
  Steamer Bag
  10/13/19 to 11/08/19
  795631808131
  Broccoli & Cauliflower with Butter – 16 oz
  Small Generic clear label on Q & E Steamer bag
  Steamer Bag
  10/13/19 to 11/08/19
  795631808186
  Tomato, Carrot, Broccoli & Snap Pea- 13 oz
  Crazy Fresh/Quick&Easy/Plain Label
  Clear Plastic Container
  10/10/19 to 11/10/19
  795631808193
  Tomato, Radish Broc & Cauli – 13 oz
  Crazy Fresh/Quick&Easy/Plain Label
  Clear Plastic Container
  10/10/19 to 11/10/19
  795631808299
  Veggie Tray w/Dip-1.75 lbs
  Crazy Fresh/Quick&Easy/Plain Label
  Plastic Container
  10/10/19 to 11/08/19
  795631809312
  Veggie Tray W/Ranch Dip – 3#
  Crazy Fresh
  Plastic Container
  10/10/19 to 11/08/19
  795631810011
  Riced Broccoli
  Crazy Fresh/Quick&Easy/Plain Label
  Plastic Container
  10/10/19 to 11/10/19
  795631810097
  Short Cut Stir Fry Blend – 12 oz
  Quick&Easy/Plain
  Plastic Bag
  10/10/19 to 11/10/19
  795631812008
  Short Cut Stir Fry Blend – 12 oz
  Crazy Fresh
  Plastic Bag
  10/10/19 to 11/08/19
  795631818611
  Veg Tray W/Dip- 1.5 lbs
  Crazy Fresh/Quick&Easy/Plain Label
  Plastic Container
  10/10/19 to 11/10/19
  795631827095
  Fresh Veggie Value Bowl -2.5#
  Crazy Fresh/Quick&Easy/Plain Label
  Plastic Bowl
  10/10/19 to 11/10/19
  795631827149
  Veggie Blend With Dip- 12 oz
  Crazy Fresh/Quick&Easy/Plain Label
  Plastic Container
  10/10/19 to 11/10/19
  795631827200
  Vegetable Tray with Veggie Dip-3#
  Crazy Fresh/Quick&Easy/Plain Label
  Plastic Container
  10/10/19 to 11/10/19
  795631827309
  Veggie Tray With Radishes
  Crazy Fresh/Quick&Easy/Plain Label
  Plastic COntainer
  10/10/19 to 11/10/19
  See accompanying images of labels.
  Affected product was delivered to retail stores in Minnesota, Wisconsin, North Dakota, South Dakota, Illinois, Indiana, Michigan, Iowa, Montana, Nebraska, and Wyoming.
  Retailers have been instructed to remove affected products from store shelves and inventory immediately. Consumers are urged to immediately throw product away and not consume.
  Consumers with questions may contact the company at: customerservice@russdaviswholesale.com or 877-433-2173 between 8:00 am and 5:00pm central standard time.
• Taher, Inc., in conjunction with Mann Packing Co., as part of a multi-state recall due to the potential risk of Listeria monocytogenes, in an abundance of caution is announcing a voluntary recall of vegetable cups served in select locations in Minnesota.Listeria monocytogenes is an organism that 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.This recall impacts only the 7.5oz Fresh Seasons Kitchen Veggie & Ranch Cup containing cauliflower sold between October 30, 2019 and November 4, 2019 in select cafeterias and vending machines in Minnesota. The cup has a UPC number of 8 10106 020334 and a sell by date of November 11, 2019.No illnesses or injuries have been reported to date in connection with either the Mann Packing Co. or Taher, Inc. voluntary recall. These products have been recalled out of an abundance of caution.
• Vitamin Cottage Natural Food Markets, Inc., a Lakewood, Colorado-based natural grocery chain, is recalling Natural Grocers brand 2-pound Organic Soybeans because they have the potential to contain mold. Consumers who may have purchased this product are advised to discontinue use and either throw it away or return it to the store for credit or refund.
  The recalled product is packaged in clear plastic bags weighing 2 pounds and bearing the “Natural Grocers” label. Only packages bearing 19-168 and 19-205 as the packed-on dates are subject to recall. The packed-on date can be found in the bottom left-hand corner of the label.
  The potential for contamination was noted after routine testing by the company revealed the presence of mold.
  Production of the product has been suspended while the Food and Drug Administration and the company continue their investigation into the source of the problem.   UPC Code
  Description
  Packed on Dates
  000080663607
  Organic Soybeans 2 LB
  19-168 & 19-205
  The product was distributed to 154 Natural Grocers’ stores located in Arkansas, Arizona, Colorado, Iowa, Idaho, Kansas, Louisiana, Minnesota, Missouri, Montana, Nebraska, Nevada, New Mexico, North Dakota, Oklahoma, Oregon, Texas, Utah, Washington and Wyoming. Consumers can find the specific locations of Natural Grocers’ stores in those states at: https://www.naturalgrocers.com/store-directory
• Creative Food Processing, a Santa Clara, Calif. establishment is recalling approximately 1,941 pounds of raw chicken products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains wheat, a known allergen, which is not declared on the product label.
  The raw chicken skewer items were produced from April 16, 2019 to Nov. 6, 2019. The following products are subject to recall: [View Labels (PDF only)]
  1-lb. sealed trays containing “GREEN MEADOWS PREMIUM MEAT CUTS Savory Chicken Boti Kebab” with use or freeze by dates from May 1, 2019 to Nov. 20, 2019 represented on the label.
  The products subject to recall bear establishment number “P-6052” inside the USDA mark of inspection. These items were shipped to retail grocery stores in California.
  The problem was discovered during routine FSIS inspection.
  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 consumers’ refrigerators or 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.
  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 and members of the media with questions about the recall can contact Ananya Dasgupta, Director of Operations, CalPerf Inc., at calperf.info@gmail.com.
• The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert because New York Style Sausage Co., a Sunnyvale, Calif. establishment, sold 77 pounds of raw pork sausage products that were misbranded. The products contain sesame seed, an allergen, which is not declared on the product label. A recall was not requested because it is believed that products are no longer available for consumers to purchase.
  The raw pork sausage items were produced on Oct. 15, 2019. The following products subject to the public health alert are: [View labels (PDF only)]
  16-oz. plastic wrapped packages containing “SHANNON VALLEY IRISH BRAND Jumbo Pub Style PORK BANGERS.” The product is labeled “Re-freeze or keep refrigerated” and does not bear a use by or sell by date.
  16-oz. plastic wrapped packages containing “SHANNON VALLEY TRADITONAL IRISH BRAND PORK BANGERS.” The product is labeled “Re-freeze or keep refrigerated” and does not bear a use by or sell by date.
  The products subject to the public health alert bear establishment number “EST. 9027” inside the USDA mark of inspection. These items were shipped to a distributor for direct sales to consumers in California.
  The problem was discovered by FSIS during routine inspection label verification activities.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
  FSIS is concerned that some product may be frozen and 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.
  Consumers and members of the media with questions about the public health alert can contact Pasquale Bitonti, vice president of New York Sausage Co., at (408) 745-7675.
• Mill Stream Corp. (Sullivan Harbor Farm) of Hancock, Maine is voluntarily recalling ten lots of Cold Smoked Salmon because it has 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 illnesses have been reported to date.
  The recall was initiated because the product’s water phase salt (WPS) tested below 3.5%. This was discovered upon re-review of laboratory certificates, which were found to have incorrectly reported WPS levels. Labeling instructions state to keep refrigerated at or below 38ºF and that the product may be frozen. Because the WPS is under 3.5% the product must remain frozen until ready to consume. Product stored in the refrigerator after thawing has the potential to be contaminated with Clostridium botulinum.
  The recalled product was sold between March 6, 2019 and September 17, 2019 in vacuum sealed packages in the following sizes: whole salmon side, 2 lb., 1 lb., 8 oz., and 4 oz. The affected product is marked with the following lot numbers marked on the back of the packages: 7049, 7050, 7051, 7052, 7054, 7056, 7058, 7060, 7062, 7066.
  The smoked salmon products were sold and distributed in ME, MA, VT, RI, NY, CT, PA, NJ, OH, UT, IA, TN, MN,CO,FL, AZ,WI, WA, GA, IL, VA, MI, TX. The products sold were through retail, wholesale and online orders.
  The affected product was sold frozen by Mill Stream Corp, but may have been thawed by retailers before sale. Consumers who purchased the product frozen are advised to keep it frozen until ready to use and thaw under refrigeration immediately before use. If a consumer has refrigerated product subject to the recall, they should dispose of it immediately even if it does not look or smell spoiled.
  Consumers with questions may contact the company at 207-266-0621, Monday-Friday, 8am-5pm EST.
• Recall: 38 Lots of Ranitidine Tablets, Ranitidine Capsules and Ranitidine Syrup by Aurobindo Pharma USA: Recall – Due to the Detection of Nitrosodimethylamine Impurity   ISSUE: Aurobindo Pharma USA, is conducting a voluntary recall of:
  • 1 lot of Ranitidine Tablets 150mg to the retail level.
  • 37 lots of Ranitidine Capsules 150mg, Ranitidine Capsules 300mg and Ranitidine Syrup 15mg/mL to the consumer level.
  All recalls are due to the detection of NDMA (Nitrosodimethylamine) Impurity in the finished product. The impurity detected is N-nitrosodimethylamine (NDMA), which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, and has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC) classification. For a complete list of those products being recalled, please read the recall alert.To date, Aurobindo Pharma USA, has not received any reports of adverse events related to this recall.
• Ezzo Sausage Company, a Columbus, Ohio establishment, is recalling approximately 25,115 pounds of sausage products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The ready-to-eat sausage products were produced on Oct. 29, 2019, Oct. 30, 2019 and Nov. 5, 2019. This spreadsheet contains a list of the products subject to the recall. [View labels (PDF only)
  The products subject to recall bear establishment number “EST. 1838A” inside the USDA mark of inspection. These items were shipped to distribution centers in Indiana and Ohio.
  The problem was discovered when the firm notified FSIS of a positive sample result for Listeria monocytogenes.
  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.
  Media and consumers with questions regarding the recall can contact Darryl Thompson, V.P Business Development, Ezzo Sausage Company, at (614) 445-8841.
• The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat entrees due to the products containing FDA-regulated ingredients that have been recalled by Mann’s Packing Co. due to possible Listeria monocytogenes contamination. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers are aware that these products should not be consumed.
  Congressional and Public Affairs
  Buck McKay (202) 720-9113
  The following products have been identified as containing products involved in the FDA recall:
  12-oz. sealed plastic trays containing “CRAZY FRESH Quick & Easy Broccoli Cheddar with Bacon” with sell by dates of 10/13/19 – 11/08/19 represented on the label.12-oz. sealed plastic trays containing “KOWALSKI’S Quick & Easy Broccoli Cheddar with Bacon” with sell by dates of 10/13/19 – 11/08/19 represented on the label.12-oz. sealed plastic trays containing “quick & easy Meals Quick & Easy Broccoli Cheddar with Bacon” with sell by dates of 10/13/19 – 11/08/19 represented on the label.
  15.8-oz. clear plastic clamshell packages containing “BUTTER CHICKEN amazon go Butter Chicken with Turmeric Rice” with best by dates through November 6, 2019 represented on the label.
  13.05-oz. plastic clamshell packages containing “BROCCOLI CRUNCH POWER BOWL amazon go BROCCOLI CRUNCH POWER BOWL WITH CHICKEN” with best by dates through November 6, 2019 represented on the label.
• This recall is connected to a voluntary recall of vegetable products announced by Mann Packing Co., Inc. on November 3 after they were notified by the Food and Drug Administration and the Canadian Food Inspection Agency of potential contamination.
  How to identify the recalled product:
  Veggie Power Blend
  Sold on the Self-Serve Cold Bar between 9/29/2019 and 11/04/2019
  Tofu Shiitake Slaw
  Sold on the Self-Serve Cold Bar between 9/29/2019 and 11/04/2019
  Refund information:
  Customers may return to the Service Desk for a full refund.
  For more information, contact:
  Wegmans Food Markets at 1-855-934-3663 Monday through Friday from 8:00 AM – 7:00 PM or Saturday and Sunday from 8:00 AM – 5:00 PM
• You Chang Trading, Inc., a Brooklyn, N.Y. establishment, is recalling an undetermined amount of raw Siluriformes fish filet products labeled as Tilapia that were not presented for FSIS import re-inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The frozen, raw Siluriformes fish filet items labeled as Tilapia were produced between Nov. 13, 2018 and Jan. 5, 2019. The following products are subject to recall: [View labels (PDF only)
  22-lb. white cardboard boxes containing “CONWAY TILAPIA FILLETS PRODUCT OF HONGKONG” and lot codes 20181113, 20181203, or 20190105 and sell by dates of 11/16/2020, 12/03/2020, or 01/05/2021 represented on the label.
  These items were shipped to distributor and retail locations in Massachusetts, New Jersey, New York, and Pennsylvania.
  The problem was discovered by FSIS during routine surveillance.
  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.
  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 about the recall can contact Yang Zhou Lu, President, You Chang Trading Inc., at (718) 633-7816. Members of the media with questions about the recall can contact Michael Lu, Translator, You Chang Trading Inc., at (917) 833-0307.
• The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat entrees due to the products containing FDA-regulated ingredients that have been recalled by Mann’s Packing Co. due to possible Listeria monocytogenes contamination. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers are aware that these products should not be consumed.
  The following products have been identified as containing products involved in the FDA recall:
  12-oz. sealed plastic trays containing “CRAZY FRESH Quick & Easy Broccoli Cheddar with Bacon” with sell by dates of 10/13/19 – 11/08/19 represented on the label.12-oz. sealed plastic trays containing “KOWALSKI’S Quick & Easy Broccoli Cheddar with Bacon” with sell by dates of 10/13/19 – 11/08/19 represented on the label.12-oz. sealed plastic trays containing “quick & easy Meals Quick & Easy Broccoli Cheddar with Bacon” with sell by dates of 10/13/19 – 11/08/19 represented on the label.
  15.8-oz. clear plastic clamshell packages containing “BUTTER CHICKEN amazon go Butter Chicken with Turmeric Rice” with best by dates through November 6, 2019 represented on the label.
  13.05-oz. plastic clamshell packages containing “BROCCOLI CRUNCH POWER BOWL amazon go BROCCOLI CRUNCH POWER BOWL WITH CHICKEN” with best by dates through November 6, 2019 represented on the label.
  FSIS is concerned that some product may be in consumers’ refrigerators. Consumers that have these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
  There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care 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 can occur 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.
• Quite a few pills/caps size amts etc are listed! Call your Doctor! Aurobindo Pharma USA, Inc. is conducting a voluntary recall of 1 lot of Ranitidine Tablets 150mg to the retail level and 37 lots of Ranitidine Capsules 150mg, Ranitidine Capsules 300mg and Ranitidine Syrup 15mg/mL to the consumer level due to the detection of NDMA (Nitrosodimethylamine) Impurity in the finished product. The impurity detected is N-nitrosodimethylamine (NDMA), which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, and has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC) classification. To date, Aurobindo Pharma USA, Inc. has not received any reports of adverse events related to this recall.
  Ranitidine is a competitive, reversible inhibitor of the action of histamine at the histamine H2 receptors found in gastric parietal cells. This results in decreased gastric acid secretion and gastric volume, and reduced hydrogen ion concentration. Uses are:
  Relieves heartburn associated with acid indigestion and sour stomach.
  Prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages.
  Patients who prescribed or are taking Ranitidine Tablets 150mg, Ranitidine Capsules 150mg, Ranitidine Capsules 300mg and Ranitidine Syrup 15mg/mL should continue taking their medication. Patients should contact their pharmacist or physician who can advise them about an alternative treatment prior to returning their medication.
  The products subject to recall are listed below and are packaged in bottles. The product can be identified by checking the product name, manufacturer details and batch or lot number on the bottle containing these products. Ranitidine Tablets 150mg, Ranitidine Capsules 150mg, Ranitidine Capsules 300mg and Ranitidine Syrup 15mg/mL were distributed nationwide to Aurobindo Pharma USA, Inc. and AuroHealth wholesale and distributor customers 28 September 2018 through 19 September 2019. Qualanex, on behalf of Aurobindo Pharma USA, Inc. will be notifying its distributors and customers by phone and in writing to immediately discontinue distribution of the specific lots being recalled and to notify their sub-accounts. Aurobindo Pharma USA, Inc. is arranging for return of all recalled products to Qualanex. Instructions for returning recalled products are given in the recall letter.
  Consumers with medical questions regarding this recall or to report an adverse event can contact Aurobindo Pharma USA, Inc. at:
  1-866-850-2876 Option 2
  pvg@aurobindousa.com
  Consumers should also contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
  Any general questions regarding the return of this product please contact Qualanex at 1-888-504-2014 or email recall@qualanex.com (live calls received 7:00 am to 4:00
• Simmons Prepared Foods, Inc., a Gentry, Ark. establishment, is recalling approximately 2,071,397 pounds of poultry 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 poultry items were produced from Oct. 21, 2019 through Nov. 4, 2019. This spreadsheet contains a list of the products subject to the recall.[View labels (PDF only)]
  The products subject to recall bear establishment number “P-1949,” “P- 486” or “P-5837” inside the USDA mark of inspection. These items were shipped to institutions in Alabama, Arizona, Arkansas, California, Georgia, Minnesota, Oklahoma and Pennsylvania.
  The problem was discovered by Simmons Prepared Foods, Inc. establishments during further processing.
  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 institutional freezers. 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, the retail distribution list(s) will be posted on the FSIS website at http://www.fsis.usda.gov/recalls.
  Consumers with questions about the recall can contact Donald Miller, senior vice president of sales at Simmons Prepared Foods, Inc., at (888) 831-7007. Members of the media with questions about the recall can contact Donny Epp, senior director of communications at Simmons Prepared Foods, Inc., at (479) 215-2626.
• GHNW, LLC of Clackamas, OR is voluntarily recalling Mushroom Stir Fry Blend 10 oz. tray and Stir Fry Blend 16 oz. tray that were produced using Broccoli Slaw that is being recalled by Mann Packing Co., Inc. 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.
  At this time, we are not aware of any illnesses linked by health officials to this recall. No other GHNW, LLC products are affected by this recall.
  GHNW, LLC is issuing this recall out of an abundance of caution. The recalled products have “Sell By” dates of October 27, 2019 to November 8, 2019, which can be found printed in black ink on the front label of the product. The products affected were sold at QFC and/or Fred Meyer in Oregon and Washington State.
  Consumers who believe that they are in possession of any of the products affected by this recall should dispose of the product in an appropriate waste container.
  For any inquiries or comments, consumers with questions regarding this GHNW recall are welcome to call 888-449-9386, M-F, 9 am to 4 pm PST.
• In response to Mann Packing Co., Inc’s recall of vegetable products, Whole Foods Market is voluntarily recalling multiple products from its stores in the United States. Mann Packing issued the recall because the vegetables may be contaminated with Listeria monocytogenes. No illnesses have been reported to date.
  Listeria monocytogenes is a bacterium 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.
  View the list of items that have been affected by state.
  External Link Disclaimer
  The recall only affects products that are listed above; these products were available on salad and hot bars, chefs’ cases or packaged in plastic containers. The affected products were sold between Oct. 10, 2019 and Nov. 4, 2019.
  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.
• Mill Stream Corp. (Sullivan Harbor Farm) of Hancock, Maine is voluntarily recalling ten lots of Cold Smoked Salmon because it has 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 illnesses have been reported to date.
  The recall was initiated because the product’s water phase salt (WPS) tested below 3.5%. This was discovered upon re-review of laboratory certificates, which were found to have incorrectly reported WPS levels. Labeling instructions state to keep refrigerated at or below 38ºF and that the product may be frozen. Because the WPS is under 3.5% the product must remain frozen until ready to consume. Product stored in the refrigerator after thawing has the potential to be contaminated with Clostridium botulinum.
  The recalled product was sold between March 6, 2019 and September 17, 2019 in vacuum sealed packages in the following sizes: whole salmon side, 2 lb., 1 lb., 8 oz., and 4 oz. The affected product is marked with the following lot numbers marked on the back of the packages: 7049, 7050, 7051, 7052, 7054, 7056, 7058, 7060, 7062, 7066.
  The smoked salmon products were sold and distributed in ME, MA, VT, RI, NY, CT, PA, NJ, OH, UT, IA, TN, MN,CO,FL, AZ,WI, WA, GA, IL, VA, MI, TX. The products sold were through retail, wholesale and online orders.
  The affected product was sold frozen by Mill Stream Corp, but may have been thawed by retailers before sale. Consumers who purchased the product frozen are advised to keep it frozen until ready to use and thaw under refrigeration immediately before use. If a consumer has refrigerated product subject to the recall, they should dispose of it immediately even if it does not look or smell spoiled.
  Consumers with questions may contact the company at 207-266-0621, Monday-Friday, 8am-5pm EST.
• Rastelli Bros., Inc., doing business as Rastelli Foods Group, a Swedesboro, N.J. establishment, is recalling approximately 130,464 pounds of raw ground beef products that may be contaminated with extraneous materials, specifically plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
  The raw ground beef items were produced from Oct. 3, 2019 through Oct. 15, 2019. The following products are subject to recall: [View labels (PDF only)]
  16-oz vacuum sealed packages containing “NATURE’S RANCHER 100% GRASS FED ORGANIC GROUND BEEF 85% LEAN, 15% FAT” with case code 9276, 9283, 9287, or 9288 and use or freeze by dates of 10/24/19, 10/31/19, 11/04/19, 11/07/19, and 11/11/19.
  16-oz vacuum sealed packages containing “NATURE’S RANCHER 100% GRASS FED ORGANIC GROUND BEEF 93% LEAN, 7% FAT” with case code 9276, 9283, 9287, or 9288 and use or freeze by dates of 10/24/19, 10/31/19, 11/04/19, 11/07/19, and 11/11/19.
  The products subject to recall bear establishment number “EST. 7877-A” inside the USDA mark of inspection. These items were shipped to distribution centers and further sent to retail locations in Colorado, Connecticut, Georgia, Illinois, and Maryland.
  The problem was discovered after FSIS received consumer complaints through the USDA Meat and Poultry Hotline. The firm also notified FSIS that they received a consumer complaint directly.
  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 consumers’ refrigerators or 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.
  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.
  Consumers with questions about the recall can contact Mike Kelly, vice president of sales at Rastelli, at (856) 803-1100. Members of the media with questions about the recall can contact Raymond Rastelli, Jr., president and owner of Rastelli, at (856) 803-1100.
• Fagron Inc. is voluntarily recalling all unexpired lots of LETS GEL KIT Convenience Packs to the hospital, pharmacy and distributor level. The product has been found to potentially contain microbial contamination in the non-sterile Suturagel Methylcellulose base component of the LETS GEL KIT Convenience Packs. FDA analysis identified Bacillus fortis/Geobacillus toebii, Bacillus spp, and Bacillus circulans as contaminants in some samples obtained during an inspection of Fagron Inc.
  This non-sterile product has the potential to result in an increased chance of infection at the site of administration during open wound care. The use of this or other non-sterile products in wound treatment may increase the risk of infection, especially for immunocompromised patients, the elderly or children. To date, Fagron Inc. has not received any reports of adverse events related to this recall. Fagron Inc. places the health and well being of patients first and focuses on quality throughout our production processes. Fagron Inc. will contact all affected customers via a recall letter to arrange for the return of all products identified in the recall.
  The product is used as a topical anesthetic and is packaged in boxes containing lidocaine hydrochloride, epinephrine bitartrate, tetracaine hydrochloride, sodium metabisulfite, Suturagel Methylcellulose base, adapter cap and syringes. The affected LETS GEL KIT Convenience Pack lots include the following lot numbers and expiration dates:
  Lot Number
  Expiration Date
  18F25-U03-044296
  11/8/2019
  18F25-U04-044297
  11/8/2019
  18H22-U06-045284
  1/24/2020
  18I24-U05-045853
  11/8/2019
  18K06-U03-047041
  1/24/2020
  18K06-U04-047042
  1/24/2020
  18K27-U11-047460
  3/16/2020
  18K28-U10-047519
  3/16/2020
  19A06-U02-048182
  3/16/2020
  19A06-U03-048183
  3/16/2020
  19A16-U13-048363
  3/16/2020
  19A21-U02-048503
  3/16/2020
  19B10-U02-048787
  3/16/2020
  19B14-U05-048781
  3/16/2020
  19C05-U01-049199
  3/16/2020
  19C05-U02-049200
  3/16/2020
  19C11-U07-049451
  3/16/2020
  19C25-U02-048758
  3/16/2020
  19D07-U01-049884
  3/16/2020
  19D07-U02-049885
  3/16/2020
  19E09-U01-050298
  3/16/2020
  19E23-U01-050763
  9/11/2020
  19F16-U12-000052
  9/11/2020
  19F16-U13-000053
  10/24/2020
  19G07-U01-000357
  10/24/2020
  19G07-U02-000358
  10/24/2020
  19G21-U01-000930
  10/24/2020
  19G21-U02-000931
  12/17/2020
  19H01-U01-001172
  12/17/2020
  19H01-U02-001174
  12/17/2020
  19I03-U01-002019
  2/4/2021
  19I03-U02-002020
  2/4/2021
  19I03-U03-002021
  12/17/2020
  The product can be identified by the product packaging and labeling. The product was distributed nationwide to hospitals, pharmacies and distributors.
  Fagron Inc. is notifying its distributors and customers by phone, e-mail, and/or letter and is arranging for return of all recalled products. Hospitals, pharmacies and distributors that have LETS GEL KIT Convenience Packs which are being recalled should quarantine this material. Please immediately discontinue use or distribution of the affected lots.
  Consumers with questions regarding this recall can contact Stericycle via the following information.
  Phone: 877-448-5308 (8am – 5pm EST)
  FAX: 877-884-9410
  Email: Fagron7222@stericycle.com
  Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using the 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 relation to the Mann Packing Co. recall, we have been notified that Trader Joe’s Baby Cauliflower (SKU 66248) –– sold only in our AZ, CA, ID, NV, OR, UT and WA stores –– with the Best If Enjoyed By date codes October 11, 2019 through November 16, 2019 may have the potential to be contaminated with Listeria monocytogenes.
  No illnesses have been reported to date.
  If you have purchased any of the Baby Cauliflower with the specified date codes, please do not eat it. Instead, we urge you to discard the product or return it to any Trader Joe’s for a full refund.
  If you have any questions, you may call Trader Joe’s Customer Relations at (626) 599-3817 [Monday through Friday, 6:00 am to 6:00 pm Pacific Time].
  We sincerely apologize for the inconvenience.
  
• Mann Packing Co., Inc. announced today the voluntary recall of a series of vegetable products sold to select retailers in the United States and Canada. The voluntary recall is a response to a notification by the Food and Drug Administration and the Canadian Food Inspection Agency of a potential contamination with Listeria monocytogenes. To date, public health officials have not reported any illness associated with these products.
  Mann Packing is issuing this recall out of an abundance of caution. 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. Mann Packing will continue to work closely with the authorities to investigate the issue.
  The recalled products have “Best If Enjoyed By” date of October 11, 2019 to November 16, 2019. The full list of products and all corresponding product images are available at https://mannpackingproductlist11-2019.us
  External Link Disclaimer
  and https://mannpackingproductlist11-2019.ca
  External Link Disclaimer
  Consumers who believe that they are in possession of any of the products affected by this recall should dispose of the product in an appropriate waste container.
  For any inquiries or comments, all consumers are welcome to call the 24 hour customer service line at 1-844-927-0707 or email Mann Packing Co., Inc. at consumers@mannpacking.com
• Padrino Foods, LLC, an Irving, Texas establishment, is recalling approximately 1,931 pounds of beef tamales because the products may be misbranded, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products are labeled as beef and sirloin tamales but contain pork product inside the package.
  The fully cooked, not shelf stable beef tamales items were produced on May 8, 2019. The following products are subject to recall: [View label (PDF only)]
  60-oz. packages containing “padrino foods BEEF & SIRLOIN TAMALES Homestyle in corn husks” with lot code 2128903 and a sell-by date 12-27-19.
  The products subject to recall bear establishment number “EST. 13136” inside the USDA mark of inspection. These items were sold at retail locations in Kansas, Louisiana, Oklahoma and Texas.
  The problem was discovered by a customer who notified the firm of the misbranding error.
  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 Diane Luther, owner of Padrino Foods, LLC, at (214) 905-3444. Members of the media with questions about the recall can contact David Luther, Padrino Foods, LLC CEO, at (214) 905-3444.
• Cay Thi Queentrees Food USA, the importer of record, a Garden Grove, Calif. firm, is recalling approximately 43,848 pounds of poultry products that were imported and distributed in the United States without the benefit of FSIS import re-inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Additionally, the products were imported from Vietnam, a country ineligible to export poultry products to the U.S.
  The poultry products entered the U.S. on Jan. 2, 2019 and Jan. 25, 2019. The following products are subject to recall:[View labels (PDF only)]
  454-g packages containing “SLOW-COOKED BLACK CHICKEN GA AC TIEM CORDYCEPS SINENSIS DONG TRUNG HA THAO” with lot code H9007 and a sell-by date Jan/02/2020 or Jan/25/2020.
  454-g packages containing “SLOW-COOKED BLACK CHICKEN GA AC TIEM FIVE SPICE NGU V!” with lot code 8324/T8352 and a sell-by date Jan/02/2020 or Jan/25/2020.
  454-g packages containing “SLOW-COOKED BLACK CHICKEN GA AC TIEM GINSEN NHAN SAM” with lot code A8328 and a sell-by date Jan/02/2020 or Jan/25/2020.
  These items were shipped to retail stores in California and sold via internet/catalog sales.
  The problem was discovered by FSIS during in-commerce surveillance activities.
  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 Nguyen Le, Cay Thi Queentrees Food USA CEO, at (714) 230-5554.