• Pinnacle Foods Inc. Recalls Beef Products Due to Possible Processing DeviationPinnacle Foods Inc., a Fort Madison, Iowa establishment, is recalling approximately 32,479 pounds of heat-treated, shelf stable beef products due to a possible processing deviation that may have led to staphylococcal enterotoxin and clostridial toxin contamination.
• Greenbelt Greenhouse LTD of British Columbia, Canada is recalling all Greenbelt Microgreen products with the best before dates from 4/24/18 and 4/30/18 because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.Greenbelt Microgreen products can be identified by the Greenbelt Microgreen label (which is purple & Green) on the lid of the plastic clamshells which is clear. The best before date can be found on the bottom left corner of the label above the UPC barcode.The affected Greenbelt Microgreens brand microgreens were distributed to Whole Foods stores in Washington between 04/11/18 and 04/24/2018.

  Brand	Product	Size	UPC	Codes
  Greenbelt Microgreens	Arugula Microgreens	75 g	8 90082 00012 4	Best Before: 4/24/18 4/30/18
  Greenbelt Microgreens	Broccoli Microgreens	75 g	8 90082 00016 2	Best Before: 4/24/18 4/30/18
  Greenbelt Microgreens	Fresh Microgreen Mix	75 g	8 90082 00041 4	Best Before: 4/24/18 4/30/18
  Greenbelt Microgreens	Sweet & Crunchy Microgreen Mix	75 g	8 90082 00006 3	Best Before: 4/24/18 4/30/18
  Greenbelt Microgreens	Spicy Microgreen Mix	75 g	8 90082 00000 1	Best Before: 4/24/18 4/30/18
  Greenbelt Microgreens	Pea Shoots Microgreens	100 g	8 90082 00023 0	Best Before: 4/24/18 4/30/18
  Greenbelt Microgreens	Sunflower Microgreens	100 g	8 90082 00030 8	Best Before: 4/24/18 4/30/18

  No illnesses have been reported to date.

  The recall was the result of sampling program by Washington State Department of Agriculture (WSDA) which revealed that the Broccoli Microgreen contained the bacteria. Due to the potential risk of contamination the company has ceased the production and distribution of all product as Canadian Food Inspection Agency (CFIA) and the company continue their investigation as to what caused the problem.

  This recall is being made with the knowledge of the U.S. Food and Drug Administration and WSDA.

  If consumers are in possession of these products, they should dispose of or return them to the place of purchase.

  Consumers with questions may contact Greenbelt Greenhouse LTD at 1-519-647-1112 from Monday-Friday, 8am-4pm EST. Additionally, we can be reached by email at info@greenbeltmicrogreens.ca

• Second E. coli case in Washington linked to romaine lettuce; 84 ill nationwide http://via.q13fox.com/cxrvz  via @Q13FOX
• OC Raw Dog, LLC of Rancho Santa Margarita, CA, is recalling approximately 1,560 lbs of Chicken, Fish & Produce Raw Frozen Canine Formulation which was manufactured on 10/11/2017 with a lot number 3652 and a use by date of 10/11/18. We are voluntarily recalling because of potential contamination with Listeria monocytogenes, which can cause severe and potentially fatal infection in animals consuming the pet food, and the humans that handle the pet food and surfaces exposed to the product. Pets can be carriers of the bacteria and infect humans, even if the pets do not appear to be ill. Short-term symptoms may include high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Young children, frail or elderly people, and others with weakened immune systems are particularly vulnerable to Listeria monocytogenes infections, which can cause miscarriages and stillbirths among pregnant women. Healthy people infected with Listeria monocytogenes should monitor themselves and their pets for symptoms.Lot # 3652 of OC Raw Dog Chicken, Fish & Produce was shipped to the following states with the following associated volume with the intent to sell to Independent Specialty Retailers and in turn sold to Consumers. California – 356 lbs., Colorado – 153 lbs., Florida – 195 lbs., Maryland – 320 lbs., Minnesota – 429 lbs., Pennsylvania – 78 lbs. and Vermont – 30 lbs.This lot of OC Raw Dog Chicken, Fish & Produce was made into 3 lb. Meaty Rox Bags, 4 lb. Slider Bags, 6.5 lb. Doggie Dozen Patty Bags and 7 lb. Meaty Rox Bags. All of which have been marked with a lot number of 3652 and a USE BY DATE of 10/11/18. Each bag has this information on a sticker located on the back lower left corner of the bag.

  Product	Package Nt. Wt.	UPC No.	Bar Code
  OC Raw Dog Chicken, Fish & Produce Meaty Rox	3 lb.	022099069171
  OC Raw Dog Chicken, Fish & Produce Doggie Sliders	4 lb.	095225852640
  OC Raw Dog Chicken, Fish & Produce Doggie Dozen Patty Bag	6.5 lb.	022099069225
  OC Raw Dog Chicken, Fish & Produce Meaty Rox	7 lb.	095225852756

  To date there have been no reported illnesses of dogs, cats or persons in any connection with this product. The contamination is still under investigation.

  OC Raw was notified by the FDA of the contamination after it was reported that New Jersey Department of Food and Agriculture tested the product and found it to be positive.

  The same lab who conducted the tests for Listeria also tested for Salmonella on our 3 lb. bag of Chicken, Fish & Produce Meaty Rox and the test was negative. In addition to the OC Raw Dog Chicken, Fish & Produce tests the lab conducted tests for OC Raw Dog Pumpkin Rox for Listeria monocytogenes and Salmonella and the results were negative.

  OC Raw Dog is a family owned and managed by passionate dog enthusiasts who take very seriously the safety and wellbeing of its consumers and clients. We are dedicated to producing a quality product that is safe. We are taking this contamination very seriously and have sent multiple samples of machines, utensils, packaging equipment and freezers to insure there is no contamination at our facility. We have also sent several individual ingredients to insure we are using safe ingredients and the food we produce is done so in a safe environment. All samples have returned negative for listeria.

  There was product at two of the seven distribution locations. The product has been pulled from inventory and destroyed. It is possible there might be a few bags at retailers or at home with consumers. We strongly urge anyone who has purchased OC Raw Dog’s Chicken, Fish & Produce to check the lot number.

  Consumers who have purchased product with lot 3652 are urged to return it to the Retailer where it was purchase for a full refund. Consumers with questions may contact the company at 1-844-215-DOGS Monday – Friday 8am – 5pm PST

• As a precaution, the Ziegenfelder Company of Wheeling, WV is voluntarily recalling approximately 3,000 cases of Budget $aver Cherry Pineapple Monster Pops and Sugar Free Twin Pops because the products have the potential to be contaminated with Listeria monocytogenes.

  Listeria can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as fever, headache, stiffness, nausea, abdominal pain and diarrhea, but Listeria infection can cause miscarriages and stillbirths among pregnant women.

  The ice pops were distributed to retail grocers and distributors in the states of Alabama, Arkansas, Florida, Maine, Missouri, Nebraska, Nevada, New Mexico, New York, Ohio, Oklahoma, Texas, Utah, Washington and Wyoming. Product was delivered during a 15-day period from April 5 through April 19, 2018.

  No illnesses or incidents involving the product have been reported to date.

  The frozen products were sold 12 to a package under the brand names Budget $aver Cherry Pineapple Monster Pops and Sugar Free Twin Pops. The Cherry Pineapple Monster Pops carry the UPC code 0-74534-84200-9, and have lot codes D09418A through D10018B. The Sugar Free Pops carry the UPC code 0-74534-75642-9, and have lot codes D09318A through D10018B. Below are front and back representations of the packaged products as they appear in stores.

  The voluntary recall was the result of a routine state inspection of the company’s Denver production facility which found Listeria monocytogenes in environmental samples collected by the inspector. The Ziegenfelder Company has ceased the production and distribution at the plant as the state of Colorado and the company continue their investigation as to what caused the problem.

  Consumers who have purchased the affected ice pops are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-888-683-0379, Mon-Fri 8am to 8pm EST.

• NxtGen Botanicals Maeng Da Kratom by NGB Corp.: Recall – Possible Salmonella ContaminationAUDIENCE: ConsumerISSUE: NGB Corp. of West Jordan, Utah is voluntarily recalling NxtGen Botanicals Maeng Da Kratom labeled bottles of encapsulated product because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.One illness has been reported to date and the recall was initiated after NGB Corp. was notified of positive Salmonella test results by FDA. NGB Corp. has identified the supplier and source of contaminated product and has ceased the production and distribution of the product.Distribution of an estimated 1,108 units were sold directly to 22 retailers in Utah, 2 in Massachusetts, and 1 in each of Arizona, Georgia, Minnesota, and California. The lot number can be found on the bottom of each bottle. The possibly affected products bear the lot #171409 and are packaged in plastic sealed bottles sold in 500-miligram capsules.BACKGROUND: Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis.RECOMMENDATION: Consumers who may be in possession of potentially contaminated products are advised not to consume products labeled NxtGen Botanicals Maeng Da Kratom. All products associated with this recall should be returned to NGB Corp. for a full refund. Customers can return product to the place of purchase for a full refund and retail stores will receive a full refund from NGB Corp. within 14 business days. Customers with questions about this issue should contact NGB Corp. anytime by e-mail at nxtgenbotanicals@gmail.com or via phone at (323) 813-5428 from 8:00 a.m. to 5:00 p.m. MST.Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:
  • Complete and submit the report Online: www.fda.gov/MedWatch/report
  • 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

  Read the MedWatch Safety Alert, including a link to the FDA Drug Safety Communication, at: https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm605182.htm

• Superior Foods Company located in Kentwood, Michigan is voluntarily recalling a specific lot of Smoked Salmon Spreads (487 lbs.) that were produced on March 26, 2018. This voluntary action is being undertaken in cooperation with the U.S. Food and Drug Administration and the Michigan Department of Agriculture and Rural Development.Listeria monocytogenes was identified through routine inspection and testing by MDARD.The products in question could potentially be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, pregnant women and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages, stillbirths and fatal infection in pregnant women. People experiencing these problems should seek immediate medical attention.Products covered by this voluntary recall were distributed in Michigan, Indiana, Illinois, Ohio, and Minnesota, and include only those products listed below, currently in distribution and for sale. Products were sold in retail grocery stores and some food service businesses. Specific product names and further product information is listed below.No other Superior Foods Company retail or food service-branded products are impacted by this voluntary recall.The following products are included in this product recall:Smoked Salmon Spread
  5 lb. bulk units – Code Number: 68487 – Sell by Date: 4/25/18 – Lot Number 0728-2
  UPC #043823684873Simply Superior Smoked Salmon Spread
  6X5 oz units – Code Number: 92379 – Sell by Date: 4/25/18 – Lot Number 0728-2
  UPC #043823923798Morey’s Smoked Salmon Spread
  6×6 oz units – Code Number: 92503 – Sell by Date: 4/25/2018 – Lot Number 0728-2
  UPC #043823925037Superior Foods Company is working with our customers to remove the products from store shelves and distribution. Consumers who have purchased these items are advised to discard them or return them to the store where originally purchased for a full credit.Consumers with questions may contact Scott Ruth at 616-698-7700.Superior Foods Company will be contacting our customers that have received this specific lot code that are impacted by this recall.
• World’s Best Cheeses of Armonk, NY is recalling 22 cases of Formagerie de la Brie brand, l’Explorateur soft ripened cheese because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.The Formagerie de la Brie brand, l’Explorateur, soft ripened cheese made from pasteurized milk was distributed in NY, NJ, CT, MD, UT, CO, SC, PA, TX and Washington D.C. through retail stores beginning February 28, 2018 through April 13, 2018. The Explorateur product comes in a 250g (8.8 oz.), clear plastic package marked with lot #’s H036, H038, H043 and H044.No illnesses have been reported to date by public health authorities.The cheese was manufactured by Fromagerie de la Brie of St. Simeon, France. World’s Best Cheeses was one of several importers notified by their French Consolidator of a suspicion for Listeria monocytogenes. World’s Best Cheeses is taking these steps because of our dedication to providing quality foods, and that must start with ensuring the safety of all the food we import and distribute. This recall is being undertaken with the knowledge of the FDA.Consumers should not consume the product, and should discard it or return the product to the store for refund. World’s Best Cheeses representatives have already been in contact with their retail stores that received product and requested that they remove the recalled product from store shelves and inventory and that no product is available for consumer purchase.Consumers with questions may contact World’s Best Cheeses at Recall@wbcheese.com or 914 273-1400 Monday- Friday from 8:00am – 5:00pm.
• TruPet, LLC of Milford, OH, is voluntarily recalling a limited amount of Boost Me Mighty Meaty Beef Topper Meal Enhancer because the products have the potential to be contaminated with Salmonella. The recall is limited to 400 cases of the product, as identified below.The following affected “Boost Me” products were distributed in the continental USA via online retailer Chewy.com and TruDog.com through direct delivery:Affected product can be identified by comparing the following lot number: “Boost Me Mighty Meaty Beef Topper Meal Enhancer” with “lot number #20190531 13815 “.No products other than the specific product identified above are subject to this voluntary recall.Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.The recall is being issued in an abundance of caution following the FDA’s collection of a retail sample from a single batch which tested positive. No illnesses have been reported to date.Consumers who have purchased Boost Me Mighty Meaty Beef Topper Meal Enhancer are urged to return effected product to the place of purchase for a refund. Consumers with questions may call the company at 800-476-8808 for additional information.
• NutriZone, LLC of Houston, Texas is expanding its recall of various kratom dietary supplements to additional lot numbers, which contain the same source material as the original recalled lots. The expanded recall is being conducted out of an abundance of caution.The recall of dietary supplements is due to the potential for contamination with Salmonella. Salmonella, is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.The dietary supplements are labeled and packaged as follows:

  Product Name	Net Quantity (Capsules Per Container)	Lot Number	Packaging
  Pain Out Maeng Da	36	Pouch	All
  Pain Out Thai	108	Bottle	10960-D
  Pain Out Malay	324	Bottle	10958-I
  Nirvanio Green Malay	25	Bottle	10958-C
  Nirvanio Special Reserve Kratom Blend	50	Bottle	10796
  Nirvanio Special Reserve	100	10795	Bottle
  Nirvanio Maeng Da	100	10957-A	Bottle
  Nirvanio Maeng Da	50	10957-B	Bottle
  Nirvanio Maeng Da	25	10957-C	Bottle
  Cali Maeng Da	100	10957-D	Bottle
  Cali Maeng Da	200	10957-E	Bottle
  Cali Maeng Da	300	10957-F	Bottle
  Pain Out Maeng Da	108 and 324	10957-G	Bottle
  Pain Out Maeng Da	216	10957-H	Bottle
  Nirvanio Green Malay	100	10958-A	Bottle
  Nirvanio Green Malay	50 (labeled and unlabeled)	10958-B	Bottle
  Cali Green Malay	100	10958-D	Bottle
  Cali Green Malay	200	10958-E	Bottle
  Cali Green Malay	300	10958-F	Bottle
  Pain Out Green Malay	108	10958-G	Bottle
  Pain Out Green Malay	216	10958-H	Bottle
  Cali Thai	100	10960-A	Bottle
  Cali Thai	200	10960-B	Bottle
  Cali Thai	300	10960-C	Bottle
  Pain Out Thai	216 (labeled and unlabeled)	10960-E	Bottle
  Pain Out Thai	324	10960-F	Bottle
  Nirvanio Maeng Da	50	10889	Bottle
  Nirvanio Green Malay	100	10890	Bottle
  Nirvanio Bali	50	10891	Bottle

  Attached are images of product labels to aide in identifying product associated with this recall. Lot numbers can be found on the packaging near the Nutrition Facts Panel.

  The products were sold in Pennsylvania, Oklahoma, Washington, Missouri, Florida, Mississippi, California and Texas.

  No illnesses have been reported to date in connection with this problem.

  The potential for contamination was noted after routine sampling and testing by the FDA revealed the presence of Salmonella.

  Consumers who have purchased the products listed above should discontinue use of the product and may return the unused portion to the place of purchase for a full refund. Consumers with questions may contact NutriZone, LLC, at 1-800-936-7936, Monday through Friday, 9am-5pm Central Standard time.

  Link to Original Recall

• Viable Solutions of Nampa, ID has initiated a recall of certain Kratom-containing powder products, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.The potentially affected powder products are packaged in kaft paper, foil-lined heat sealed pouches and sold in 25 grams, 100 grams, 250 grams, and 1000 grams sizes. The units were sold directly to consumers nationwide in January and February of 2018 via company websites. The products description are as follows:Recall Product Identification:

  Brand	Product Name	Net Wt.
  Herbal-Salvation.com	Mitragyna Speciosa Leaf Powder-Red Vein Sumatra	25 grams, 100 grams, 250 grams, 1000 grams
  Herbal-Salvation.com	Mitragyna Speciosa Leaf Powder-Red Vein Bali	25 grams, 100 grams, 250 grams, 1000 grams
  Herbal-Salvation.com	Mitragyna Speciosa Leaf Powder-Green Horn	25 grams, 100 grams, 250 grams, 1000 grams
  Herbal-Salvation.com	Mitragyna Speciosa Leaf Powder-Thai Maeng Da	25 grams, 100 grams, 250 grams, 1000 grams

  The lot numbers being recalled can be found on the packaging and are as follows:

  RVS1380182301
  RVB1380182201
  GVH1380171512
  MD13120181601

  The company has been notified by the Michigan Department of Health and Human Services (MDHHS) that certain lots of the product were tested positive for Salmonella. While the Salmonella has not been traced to Viable Solutions, out of an abundance of caution and concern for the public health, Viable Solutions has initiated this recall. Viable Solutions has identified the supplier and source of the potentially contaminated product and has ceased production and distribution of the potentially contaminated product. Working in cooperation with the FDA, the company will destroy all recalled product upon return.

  Consumers who may be in possession of potentially contaminated products are advised not to consume products from those LOT numbers. All products associated with this recall should be returned to Viable Solutions for a full refund. Customers can return product to company for a full refund within fourteen (14) days by contacting Viable Solutions at recall@herbal-salvation.com.

• 029-2018, Good Foods Group, LLC Recalls Ready-To-Eat Chicken Products Due to Misbranding and Undeclared Allergen (Apr 3, 2018).
• 033-2018, Fresh Foods Manufacturing Co. Recalls Ready-To-Eat Salad Products Due to Possible E. coli O157:H7 Contamination (Apr 14, 2018)
• Through an abundance of caution Rose Acre Farms of Seymour, Indiana is voluntarily recalling 206,749,248 eggs because they have the potential to be contaminated with Salmonella Braenderup, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals infected with SalmonellaBraenderup can experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella Braenderup can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.The eggs were distributed from the farm in Hyde County, North Carolina and reached consumers in the following states: Colorado, Florida, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, Virginia, and West Virginia through retail stores and restaurants via direct delivery.22 illnesses have been reported to date.The affected eggs, from plant number P-1065 with the Julian date range of 011 through date of 102 printed on either the side portion or the principal side of the carton or package, as follows:

  Lot Codes 011 – 102

  Item Description	Carton UPC
  COUNTRY DAYBREAK A LARGE X 30 DOZEN	077236000302
  COUNTRY DAYBREAK A LARGE X15 DOZEN	077236000302
  COUNTRY DAYBREAK A JUMBO X24 DOZEN	077236000500
  COUNTRY DAYBREAK A MEDIUM X30 DOZEN	077236000203
  COUNTRY DAYBREAK A XLARGE X30 DOZEN	077236000401
  COUNTRY DAYBREAK A JUMBO X12 DOZEN	077236000500
  FOOD LION A JUMBO X 12 DOZEN	035826089618
  FOOD LION A MEDIUM X15 DOZEN	035826089649
  FOOD LION A XLARGE X 15 DOZEN	035826089625
  FOOD LION A 18PK LARGE X15 DOZEN	035826089601
  FOOD LION A LARGE X15 DOZEN	035826089588
  FOOD LION A 6PK LARGE X 15 DOZEN	035826089632
  LOOSE A USDA SMALL X 30 DOZEN	N/A
  LOOSE A USDA MEDIUM X 30 DOZEN	N/A
  LOOSE A XLARGE X15 DOZEN	N/A
  LOOSE A XLARGE X30 DOZEN	N/A
  LOOSE A MEDIUM X 15 DOZEN	N/A
  LOOSE A MEDIUM X30 DOZEN	N/A
  LOOSE USDA AA XLARGE X30 DOZEN	N/A
  LOOSE USDA AA XLARGE X15 DOZEN	N/A
  LOOSE USDA AA LARGE X30 DOZEN	N/A
  LOOSE USDA AA LARGE X15 DOZEN	N/A
  LOOSE USDA AA MEDIUM X30 DOZEN	N/A
  LOOSE AA XLARGE X30 DOZEN	N/A
  LOOSE USDA AA LARGE PFG X 30 DOZEN	N/A
  LOOSE USDA AA LARGE PFG X 15 DOZEN	N/A
  LOOSE USDA A XLARGE X30 DOZEN	N/A
  NELMS A JUMBO X24	634181000018
  WAFFLE HOUSE LOOSE USDA A LARGE X 30 DOZEN	N/A
  CRYSTAL FARMS A MEDIUM X30	077236000203
  CRYSTAL FARMS A 18PK MEDIUM X 30	077236000258
  CRYSTAL FARMS A 2.5 DOZ MEDIUM X 25	077236000124
  COUNTRY DAYBREAK A XLARGE X15 DOZEN	077236000401
  COUNTRY DAYBREAK USDA GRADE A XLARGE X 240 DOZEN PULP	077236700400
  COUNTRY DAYBREAK USDA GRADE A LARGE RACK X 240 DOZEN PULP	077236700301
  COBURN FARMS A MEDIUM MP X 30 DOZEN	051933182608
  COBURN FARMS A LARGE X 30 DOZEN	051933190801
  COBURN FARMS A 18PK LARGE X 30 DOZEN	051933182509
  SUNSHINE FARMS A JUMBO X 12 DOZEN	804879457336
  GLENVIEW USDA AA LOOSE LARGE (6-2.5 FLATS) X 15 DOZEN	N/A
  GLENVIEW USDA AA LOOSE LARGE (12-2.5 FLATS) X 30 DOZEN	N/A
  GLENVIEW USDA AA LOOSE MEDIUM (6-2.5 FLATS) X 15 DOZEN	N/A
  GLENVIEW USDA AA LOOSE XLARGE (6-2.5 FLATS) X 15 DOZEN	N/A
  GLENVIEW USDA AA LOOSE MEDIUM (12-2.5 FLATS) X 30 DOZEN	N/A
  GLENVIEW USDA AA LOOSE XLARGE (12-2.5 FLATS) X 30 DOZEN	N/A
  GREAT VALUE GRADE A USDA 18PK XLARGE X 24 DOZEN RPC	078742127132
  GREAT VALUE GRADE A USDA 12PK XLARGE X 24 DOZEN RPC	078742127128
  GREAT VALUE GRADE A USDA TWIN 18PK LARGE X 24 DOZEN RPC	078742127101
  GREAT VALUE GRADE A USDA 6PK LARGE X 15 DOZEN	078742127095
  GREAT VALUE GRADE A USDA 12PK MEDIUM X 15 DOZEN	078742127224
  GREAT VALUE GRADE A USDA 12PK LARGE X 24 DOZEN RPC	078742127071
  GREAT VALUE GRADE A USDA 18PK LARGE X 24 DOZEN RPC	078742127088
  GREAT VALUE GRADE A 12PK JUMBO X 22 DOZEN RPC	078742127149
  GREAT VALUE GRADE A USDA 5DZ LARGE X 5 DOZEN	078742127118

  The voluntary recall was a result of some illnesses reported on the U.S. East Coast, which led to extensive interviews and eventually a thorough FDA inspection of the Hyde County farm, which produces 2.3 million eggs a day. The facility includes 3 million laying hens with a USDA inspector on-site daily.

  Consumers who have purchased shells eggs are urged to immediately discontinue use of the recalled eggs and to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (855) 215-5730 between the hours of 8 a.m. to 5 p.m. Eastern Standard time.

  The following is a link to the FDA Investigates Salmonella Braenderup Infections Linked to Shell Eggs from Rose Acre Farms.

• AMA Wholesale Inc. (Distributor/Re-seller), is voluntarily recalling Rhino 69 Extreme 50000 capsules to the consumer level. FDA analysis found the product to be tainted with undeclared tadalafil. Tadalafil is an active ingredient in a FDA-approved prescription drug that is used for erectile dysfunction.AMA Wholesale Inc. has not received any reports of adverse events related to this recall.Consumers who take dietary supplements for erectile dysfunction could have underlying cardiovascular disease (from diabetes, hypertension, and others). Consumers with diabetes, hypertension, high cholesterol or heart disease often take nitrates; concomitant use of nitrates and PDE5 inhibitors can lead to fatal cardiovascular collapse.Rhino 69 Extreme 50000 is used as a sexual enhancer and is packaged in single capsule, blister packs which an expiration date of 12/2022 and UPC Code: 718122071128. The product was distributed nationwide via internet sales to the customers.AMA Wholesale Inc. (Distributor/Re-seller) is notifying its customers by E-Mail and is arranging for return of the recalled product.Consumers/distributors/retailers that have purchased ‘Rhino 69 Extreme 50000’ should immediately stop the consumption and the resale of the product. Return the product to the place of purchase for a refund.AMA Wholesale Inc.’s customers with questions regarding this recall can contact the company by Phone: +1 (800) 689-6532 Monday through Friday from 9:00 am to 5:00 pm PST or E-Mail: amawholesale@hotmail.com. Consumers should contact their physician or health-care provider if they have experienced any problems that may be related to taking or using this drug product.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: www.fda.gov/medwatch/report.htm
  • Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
• R.J. Reynolds Vapor Company has voluntarily initiated a nationwide safety recall of all Vuse Vibe power units. The Company initiated the recall after receiving consumer complaints about malfunctioning batteries, which may cause the power unit to overheat and create a fire risk. The Company notified the U.S. Food and Drug Administration regarding the issue and will be working directly with the Agency on this voluntary recall.The Company has received 10 complaints related to the power unit. No injuries have been reported. The Company is voluntarily recalling the 2.6 million power units it has sold. The Company is investigating the cause of the incidents with the intent to return to the market after the issue has been resolved.All consumers who have Vuse Vibe vapor products should stop using the product and not charge the power unit. Please call 1-800-369-8200 or visit www.vusevapor.com/viberecall for information on how to return Vuse Vibe power units and receive a refund. The Company is committed to providing products of the highest quality, and we regret the inconvenience this will cause our consumers.Vuse Solo and Vuse Ciro, which use different battery components, are not included in this recall.R.J. Reynolds Vapor Company is a subsidiary of RAI Innovations Company, a subsidiary of Reynolds American Inc. Reynolds American Inc. is an indirect, wholly owned subsidiary of British American Tobacco p.l.c. R.J. Reynolds Vapor Company markets Vuse e-cigarettes. For more information, visit www.RJRVapor.com.###
• Seacrest Foods International, Inc. of Lynn, MA is voluntarily recalling 29 cases of Formagere de la Brie brand, l’Explorateur soft ripened cheese because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, pregnant women and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages, stillbirths and fetal infection among pregnant women.The Formagere de la Brie brand, l’Explorateur, soft ripened cheese made from pasteurized milk, was distributed at retail stores in Connecticut, Massachusetts, Maine, New Jersey and New Hampshire beginning on 02/06/2018 through 03/31/18. The l’Explorateur product comes in a 250g (8.8 oz), clear plastic package marked with lot # H010 or H011 on the bottom, with UPC: 3 390010 004080.No illnesses have been confirmed by public health authorities to date.The cheese was manufactured by Fromagere de la Brie of St. Simeon, France. Seacrest Foods was one of several importers notified by their French Consolidator of a potentially positive test result for Listeria monocytogenes. Seacrest Foods is taking these steps because of our dedication to providing quality foods, and that must start with ensuring the safety of all the food we import and distribute. This recall is being undertaken with the knowledge of the FDA.Consumers should not consume the product, and should discard it or return the product to the store for refund. Seacrest Foods representatives have already been in contact with retail customers that received product directly from their company and requested that they remove the recalled product from store shelves and inventories and that no product is available for consumer purchase.Consumers with questions may contact Seacrest Foods at 781-581-2066 between the hours of 9:00 a.m. and 5 p.m. EST, Monday through Friday.
• Vitakraft Sun Seed Inc. of Weston, OH, is voluntarily recalling one lot of Sunseed Vita Prima Exotics Sugar Glider Formula because it has the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.Vitakraft Sun Seed was notified on April 13, 2018, by the Michigan Department of Agriculture that Salmonella was detected in an inspection sample of product from Lot Number 271391. The tests which discovered the bacteria were part of random testing regularly performed by the State of Michigan on various consumer products, and not prompted by any consumer concerns. To date there have been no reports of illness.Products matching the specific lot number below are being recalled:

  UPC #	DESCRIPTION	LOT	Exp:
  87535-20060	Sunseed Vita Prima Exotics Sugar Glider Formula, 28oz	271391	12/20/19

  “The health and happiness of our customers and their animal companions is always our top priority. We initiated our recall procedure as soon as we were notified of this issue so we could make sure pet owners were informed,” said Brent Weinmann, President & CEO of Vitakraft Sun Seed.

  The product was distributed to the following states: CA, FL, IL, MI, NJ, NV, OH, PA, and TX, as well as Edmonton, Alberta in Canada. Retailers and distributors who received the recalled lots have been contacted and asked to pull these lots from their inventory and shelves. Consumers who have purchased a product from the recalled lot should discontinue use of the product and may return the unused portion to the place of purchase for a full refund.

  Customers who have further questions are welcome to contact Customer Service at 1-800-221- 6175, Monday through Friday between 8:30am and 5:00pm EST

• Updated information is now available. The lists of retail consignees have been posted for recalls: 024-2018, Mickey Brown, Inc Recalls Beef Burrito Products Produced Without Benefit of Inspection (Mar 20, 2018)
• Fresh Foods Manufacturing Co. Recalls Ready-To-Eat Salad Products Due to Possible E. coli O157:H7 Contamination
  Fresh Foods Manufacturing Co., a Freedom, Pa., establishment, is voluntarily recalling approximately 8,757 pounds of ready-to-eat salad products that may be contaminated with E. coli O157:H7.
• Guixens Food Group, Inc., of Miami, FL, is voluntarily recalling its ten-ounce packages of La Marinera Brand Dried Yellow Potatoes because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume this product.The above-mentioned product was distributed to and available for purchase at retail supermarkets in Florida, Georgia, South Carolina, North Carolina, California, and Tennessee.The affected La Marinera Brand Dried Yellow Potatoes come in a 10-ounce, clear plastic bag marked with “Dried Yellow Potatoes – Papa Seca AmariIla” on the label with an expiration date of July 2018. The product UPC code is 7-42287-73054-5.No illnesses or allergic reactions involving this product have been reported to date.The voluntary recall was initiated after routine sampling by the Florida State Department of Agriculture and analysis by food laboratory personnel revealed the presence of sulfites in the product, which were not declared on the label.Consumers who have purchased La Marinera Brand Dried Yellow Potatoes are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 305-634-0500, Mondays-Fridays, 9:00AM-4:00PM EST.
• Koch Foods Inc. Recalls Beef Products Due to Possible Foreign Matter Contamination
  Koch Foods, Inc., a Fairfield, Ohio establishment, is recalling approximately 119,480 pounds of beef rib-shaped patty products that may be contaminated with extraneous materials, specifically thin blue plastic pieces.
• Recall alert: Banquet Salisbury steak recalled over bone fragments https://kiro.tv/2JFpAXh 

• Maeng Da Red Powder and Capsules by Club 13: Recall – Possible Contamination With Salmonella

  AUDIENCE: Consumer

  ISSUE: Club 13 is recalling

  • 15-gram, 30-gram, 90-gram, 150-gram, and 454-gram pouches, and all bulk orders of “Maeng Da Red” kratom powder, lot # MRMD012618
  • 5-count, 25-count, 50-count, 100-count, 120-count capsule, and all bulk capsule orders of “Maeng Da Red” kratom bottles, marked with the following lot numbers on the bottom left side: MRMD013018, MRMD013118, MRMD020118, MRMD020518, MRMD022318, MRMD022718, MRMD030118, MRMD030218, and MRMD030618.
  • 5-count, 20-count, 25-count, 40-count, 50-count capsule “Maeng Da Red XS” kratom bottles, marked with the following lots numbers on the bottom left side: KRXS020718, KRXS030618, KRXS102417, KRXS110617, and KRXS120117
• J.T.M. Provisions Company Recalls Beef Products Due to Possible Foreign Matter ContaminationJ.T.M. Provisions, Co., a Harrison, Ohio establishment, is recalling approximately 14,525 pounds of fully cooked not shelf stable pulled barbequed beef products that may be contaminated with extraneous materials.
• Whole Foods Market is voluntarily recalling Explorateur French Triple Crème cheese from nine stores located in New Mexico, Texas, Arkansas, Illinois, Connecticut and New Jersey out of an abundance of caution. The cheese has 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, 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. No illnesses have been reported to date.The recall includes Explorateur French Triple Crème cheese (under the names Explorateur, Explorateur French Triple Crème Cheese and Explorateur Triple Crème French Cheese) which were both cut and packaged in clear plastic wrap, as well as sold in branded 8 oz. packages. All cheese had “sell by” dates from 02/15/2018 through 04/03/2018. The issue was discovered when Whole Foods Market was notified by a distributor of a positive test result for Listeria monocytogenes.The products sold as Explorateur French Triple Crème at the following Whole Foods Market stores with scale labels beginning with PLU code 0294317:
  • 90 E. Putnam Avenue, Greenwich, CT
  • 222 Main Street, Madison, NJ
  • 701 Bloomfield Avenue, Montclair, NJ

  The products sold as Explorateur Triple Crème French Cheese at the following Whole Foods Market stores with scale labels beginning with PLU code 203971:

  • 7245 Lake Street, River Forest, IL
  • 760 Waukegan Road, Deerfield, IL

  The products sold as Explorateur at the following Whole Foods Market stores with scale labels beginning with PLU code 293693:

  • 753 Cerillos Road, Santa Fe, NM
  • 100 Pitt Street, El Paso, TX

  The products sold as Explorateur in 8 oz. branded packages at the following Whole Foods Market stores with UPC codes 339001000408 and lot codes H10, H010, H11 or H011:

  • 753 Cerillos Road, Santa Fe, NM
  • 100 Pitt Street, El Paso, TX
  • 7245 Lake Street, River Forest, IL
  • 760 Waukegan Road, Deerfield, IL
  • 501 Bowman Road, Little Rock, AR
  • 11920 Domain Drive, Austin, TX

  Customers who purchased these products 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.

• Club 13 of St. Augustine, FL is recalling 15-gram, 30-gram, 90-gram, 150-gram, and 454-gram pouches, and all bulk orders of “Maeng Da Red” kratom powder; and 5-count, 25-count, 50-count, 100-count, 120-count capsule, and all bulk capsule orders of “Maeng Da Red” kratom bottles; and 5-count, 20-count, 25-count, 40-count, 50-count capsule “Maeng Da Red XS” kratom bottles because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.The recalled pouches and bottles of Kratom Maeng Da Red were distributed nationwide in retail stores and through mail orders.The “Maeng Da Red” powder products come in 15-gram, 30-gram, 90-gram, 150-gram, and 454-gram packages marked with lot # MRMD012618 on the back of the pouch.The “Maeng Da Red” capsule products come in 5-count, 25-count, 50-count, 100-count, 120-count capsule bottles marked with the following lot numbers on the bottom left side: MRMD013018, MRMD013118, MRMD020118, MRMD020518, MRMD022318, MRMD022718, MRMD030118, MRMD030218, and MRMD030618.The “Maeng Da Red XS” capsule products come in 5-count, 20-count, 25-count, 40-count, 50-count capsule bottles marked with the following lots numbers on the bottom left side: KRXS020718, KRXS030618, KRXS102417, KRXS110617, and KRXS120117.No illnesses have been reported to date in connection with the lot numbers subject to this recall.The potential for contamination was noted after testing by the Oklahoma Department of Agriculture. The department detected the presence of Salmonella in a 30g and 90g package of “Maeng Da Red”.Production of the product has been suspended while FDA and the company continue their investigation as to the source of the problem.Consumers who have purchased the aforementioned Maeng Da Red products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-877-922-5783, Monday through Friday, between the hours of 9:15 AM to 5:30 PM Eastern Standard Time.

• U.S. Consumer Product Safety Commission – Fast Track Recall

  Recall Date: April 15, 2018
  Recall Number: 18-137

  SPIRIT HALLOWEEN RECALLS NICKELODEON PAW PATROL MARSHALL HAT WITH FLASHLIGHT DUE TO FIRE AND BURN HAZARDS

  Recall Details

  Name of Product: Nickelodeon PAW PATROL Deluxe Marshall Hat with flashlight

  Hazard: The batteries in the flashlight can overheat, causing the flashlight to become hot, posing burn and fire hazards.

  Remedy: Refund
  Consumers should immediately take the flashlight that was sold with the hat away from children, stop using it, remove the batteries and dispose of the flashlight and contact Spirit Halloween for a full refund. Customers will be asked to provide a photo of the tag located under the ear in the hat.

  Consumer Contact: Spirit Halloween toll-free at 866-586-0155 from 9 a.m. to 5:30 p.m. ET Monday through Friday, email at GuestServices@spirithalloween.com or online at http://www.spirithalloween.com and click on product recall at the bottom of home page or http://www.spirithalloween.com/content.jsp?pageName=ProductRecall

  Units: About 20,000 (In addition, about 1,500 were sold in Canada)

  Description: This recall involves the Nickelodeon PAW PATROL Deluxe Marshall Hat sold with an accessory flashlight. The PAW PATROL Marshall hats are red with a yellow ribbon, black and white spotted dog ears and a black flash light attached to the side of the hat. The flashlight is included with the hat and they share the SKU number. Only flashlights with SKU 01292093 and date codes 1703RY01, 1603RY01, and 1503RY01 are involved in this recall.The SKU number and date codes are on the sewn in label under the ear on the hat.

  Incidents/Injuries: The firm has received three reports of the flashlight overheating and one report of an overheating flashlight in Canada. No injuries or fires have been reported.

  Sold At: Spirit Halloween stores nationwide from September 2015 through November 2017 for about $13.

  Importer: Spencer Gifts, LLC of Egg Harbor Twp, N.J.

  Distributor: Spirit Halloween, of Egg Harbor Twp, N.J

  Manufacturer: Rayland Ind. Co., of Hong Kong

  Manufactured in: China

• Bob’s Red Mill Natural Foods is voluntarily recalling 2,099 cases of Organic Amaranth Flour (22 oz.), after recent testing revealed the presence of Salmonella in a single LOT of Organic Amaranth Flour (22 oz.) with a Sell By date of Nov. 26, 2015.The recalled Organic Amaranth Flour (22 oz.) was distributed through retailers and distributors nationwide. This product and LOT was distributed in CA, FL, MI, ND, N, NY, OH, OR, TX, and WA starting June 11, 2014 and ended shipping on August 7, 2014The recalled product is Organic Amaranth Flour (22 oz.) with a Sell By Date of 11/26/2015, LOT: 169617, which can be found on the side of the package, near the top of the panel. UPC: 0 39978 00911 1While this product expired in November 2015, this product was found on the shelves of one retail store, and thus Bob’s Red Mill is recalling the product out of an abundance of caution.Consumers who have any of this affected product should not consume it and should return it to the place of purchase for credit or refund or throw it away.Other SELL BY dates and LOTS are not affected by this recall. There have been no reports of any  injuries or illnesses associated with this recall. Bob’s Red Mill issued a voluntary recall for Organic Amaranth Flour (22 oz.) after recent testing revealed the presence of Salmonella in a tested sample of Organic Amaranth Flour (22 oz.) with a Sell By date of Nov. 26, 2015. Bob’s Red Mill has commenced an investigation of the source of the problem in the Supply Chain.Bob’s Red Mill has issued this recall voluntarily. We remain committed to providing our customers with safe and healthy products.This information can be found online at www.bobsredmill.com/product-recall-notices.html Customers with any questions regarding this recall or Bob’s Red Mill products are encouraged to call the Bob’s Red Mill hotline at 800-349-2173.
•  Updated information is now available. A list of retail consignees has been posted for recall 027-2018, Target Corporation Recalls Frozen Ready-To-Eat and Non-Ready-To-Eat Meat and Poultry Products due to Possible Temperature Abuse During Transport at a Single Store on Oahu, Honolulu, HI (Mar 29, 2018).
• Good Foods Group, LLC Recalls Ready-To-Eat Chicken Products Due to Misbranding and Undeclared AllergenGood Foods Group, LLC, a Pleasant Prairie, Wis. establishment, is recalling approximately 130 pounds of fully cooked ready-to-eat curry chicken salad products due to misbranding and an undeclared allergen.
• Global Commodities Corporation, Hayward, CA is recalling one lot of Buenas Brand frozen grated coconut because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.PRODUCT NAME: GRATED COCONUT, BRAND NAME: BUENAS, DESCRIPTION: FROZEN GRATED COCONUT, UPC: 4806514650443, LOT NUMBER: 10BAAGA; 16 oz. PLASTIC BAG, PRODUCT OF THE PHILIPPINES.The coconut was shipped to retail locations in northern California beginning in February 2018.The issue was discovered through testing conducted by the State of California Department of Public Health while investigating reported illnesses.Kindly remove the above item from the shelves and return to us for proper credit.  If you have any questions, call Global Commodities Corporation at (510) 785-8885. Our hours are Monday – Friday 8:30 AM to 4:00 PM.This recall is being made with the knowledge of the Food and Drug Administration.
• 
  

  ---

  RECALL NOTICE

  Potential Foreign Matter (Glass) in Select Bottles of Stella Artois

  April 02, 2018

  

  To Our Valued Customers:

  We have been alerted by our supplier of Stella Artois that select 11.2 oz. glass bottles are being voluntarily recalled because a packaging flaw may cause a small piece of glass to break off and possibly fall into the bottles. Products with the following availability and production codes (best before date + package code + time stamp) are included in this recall:

  Stella Artois (available in our stores where beer is sold, with the exception of Utah)

  Best Before Date	Package Code	Time Stamp
  13/02/2018	49	02:00-06:00
  13/02/2018	52	22:00-23:59
  14/02/2018	52	00:00-02:00
  14/02/2018	52	22:00-23:59
  15/02/2018	52	00:00-05:00
  19/02/2018	52,55	02:00-12:00
  20/02/2018	52,55	00:00-05:00
  4/3/2018	55	21:00-23:59
  5/3/2018	55	00:00-22:00
  22/04/2018	55	22:00-23:59
  23/04/2018	55	00:00-23:59
  24/04/2018	55	00:00-03:00
  7/5/2018	55	22:00-23:59
  8/5/2018	55	0:00-11:00
  6/6/2018	49	0:80-20:00
  7/6/2018	49,52	22:00-23:59
  8/6/2018	49	00:00-13:00
  8/6/2018	52	00:00-07:00
  29/08/2018	55	04:00-10:00
  13/09/2018	55	23:00-23:59
  14/09/2018	55	00:00-22:00
  15/09/2018	55	06:00-23:59
  16/09/2018	55	00:00-18:00
  18/09/2018	55	01:00-08:00
  21/09/2018	55	03:00-23:59
  22/09/2018	55	00:00-03:00
  23/09/2018	52	09:00-23:59
  24/09/2018	52	00:00-12:00
  25/09/2018	52	12:00-23:59
  29/09/2018	52	04:00-14:00
  6/10/2018	52	19:00-23:59
  7/10/2018	52	00:00-02:00
  9/10/2018	55	02:00-07:00
  12/10/2018	49	05:00-10:00
  27/10/2018	52	01:00-13:00
  3/11/2018	55	18:00-23:59
  3/11/2018	52	20:00-23:59
  2/2/2019	55	18:00-23:59

  Stella Artois Légère (only available in our Utah stores)

  Best Before Date	Package Code	Time Stamp
  6/10/2018	55	21:00-23:59
  7/10/2018	55	00:00-02:00
  12/10/2018	52	01:00-06:00

  
  Example Production Code (Best Before Date, Package Code, Time Stamp)

  All of the potentially affected product has been removed from sale.

  Customers who have purchased any of the packages with the specified production codes are urged to not drink them, and to dispose of them or return them to any Trader Joe’s for a full refund.

  Customers with questions may contact Trader Joe’s Customer Relations at (626) 599-3817 [Monday through Friday, 6:00 am to 6:00 pm Pacific Time] or send us an email.

  We sincerely apologize for the inconvenience

• Dietary Supplements by Nutrizone: Recall – Potential for Salmonella Contamination

  ISSUE: NutriZone, LLC is recalling 4 different dietary supplements because it has the potential to be contaminated with Salmonella. The potential for contamination was noted after routine sampling and testing by the FDA revealed the presence of Salmonella.

  BACKGROUND: The products were sold in Pennsylvania, Oklahoma, Washington, Missouri, Florida, Mississippi, California and Texas.

  RECOMMENDATION: Consumers who have purchased the products listed above should discontinue use of the product and may return the unused portion to the place of purchase for a full refund. Consumers with questions may

• Kratom-containing Products by Triangle Pharmanaturals: Mandatory Recall – Risk of Salmonella

  ISSUE: FDA issued a mandatory recall order for all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC, after several were found to contain salmonella. The agency took this action after the company failed to cooperate with the FDA’s request to conduct a voluntary recall.Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:

  Read the MedWatch Safety Alert, including a link to the recall announcement, at:

  https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm603581.htm

  Complete and submit the report Online: www.fda.gov/MedWatch/report 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

• Good Foods Group, LLC Recalls Ready-To-Eat Chicken Products Due to Misbranding and Undeclared AllergenGood Foods Group, LLC, a Pleasant Prairie, Wis. establishment, is recalling approximately 130 pounds of fully cooked ready-to-eat curry chicken salad products due to misbranding and an undeclared allergen.
• MarcasUSA, LLC and Industria Farmacéutica Andromaco, S.A. de C.V. is voluntarily recalling four lots of Pasta De Lassar Andromaco Skin Protectant, 25% zinc oxide to the retail level. FDA analysis of this product confirmed that Pasta De Lassar Andromaco is contaminated with high levels of yeast, mold, and bacteria. The specific lot associated to the positive findings was never sold in the US. However, due to the amount and type of contamination the remaining four lots in the US market are being recalled out of an abundance of caution.

Use of the contaminated product could result in an increased risk of infection. To date, MarcasUSA has not received any reports of adverse events related to this recall.

PASTA DE LASSAR ANDROMACO® brand of over-the-counter (OTC) skin protectant 25% zinc oxide is indicated for treatment and prevention of diaper rash and other minor skin irritations. The affected product includes that following lots and expiration dates:

The product is packaged in 60 gram tubes sold in individual boxes (UPC #851357003004, NDC #75940-111-60). The product was distributed Nationwide via wholesale, retail and internet.  MarcasUSA, LLC is notifying its distributors and customers by direct contact and is arranging for return of all recalled products. Consumers that have the product which is being recalled should stop using and return it to the place of purchase or discard it.

Distributors and retailers that have Pasta De Lassar Andromaco® which is being recalled should return to place of purchase (wholesaler or distributor).

Consumers with questions regarding this recall can contact MarcasUSA by phone at +1-800-428-9489 or by e-mail info@pastadelassar.com on Monday – Friday from 8am to 5pm, PST.  Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

• Complete and submit the report Online: www.fda.gov/medwatch/report.htm
• Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

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

Link to Spanish Version

• PFP Enterprises LLC Recalls Raw Beef Products Produced Without Benefit of Inspection
  PFP Enterprises, LLC, also doing business as Texas Meat Packers, a Fort Worth, Texas establishment, is recalling approximately 7,146 pounds of raw beef products that were produced and packaged without the benefit of federal inspection
• NutriZone, LLC of Houston, Texas is recalling 4 different dietary supplements because it has the potential to be contaminated with Salmonella. Salmonella, is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

The dietary supplements are labeled and packaged as follows:

Attached are images of product labels to aide in identifying product associated with this recall. Lot numbers can be found on the packaging near the Nutrition Facts Panel.

The products were sold in Pennsylvania, Oklahoma, Washington, Missouri, Florida, Mississippi, California and Texas.

No illnesses have been reported to date in connection with this problem.

The potential for contamination was noted after routine sampling and testing by the FDA revealed the presence of Salmonella.

Consumers who have purchased the products listed above should discontinue use of the product and may return the unused portion to the place of purchase for a full refund. Consumers with questions may contact NutriZone, LLC at 1-800-936-7936, Monday through Friday, 9am-5pm Central Standard time.