- R. L. Zeigler Co., Inc., a Selma, Ala. establishment, is recalling approximately 11,664 pounds of ready-to-eat (RTE) poultry and meat sausage 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 products subject to recall bear establishment number “EST. P-9156S” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.The RTE Red Hot chicken and pork sausage items were produced on Nov. 29, 2018. The following products are subject to recall: [View Labels (PDF only)]
24-oz. plastic packages containing approximately 9 links of “ZEIGLER A TRADITION OF GREAT TASTE RED HOTS” with a “Use By Jan 24 19” date.
24-oz. plastic packages containing approximately 9 links of “EXTRA HOT ZEIGLER A TRADITION OF GREAT TASTE RED HOTS” with a “Use By Jan 24 19” date.Consumers and members of the media with questions about the recall can contact Jeff Berry at R. L. Zeigler Co., Inc. at (334) 410-9845. - Wegmans Food Markets, Inc. has issued a voluntary recall of fresh Cauliflower Rice, Veggie Cauliflower Rice Blend and Stir-Fry Mix with Cauliflower, sold in the produce department between 12/7/18 and 12/18/18, because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death.
The recalled products (with use-by dates of 12/11/18 through 12/22/18) are as follows:
Wegmans Cauliflower Rice, 1 lb. pkg. UPC #25313500000
Wegmans Cauliflower Rice, 8 oz. pkg. UPC #25307200000
Wegmans Stir Fry Blend (with cauliflower), 1 lb. pkg. UPC #25335800000
Wegmans Veggie (cauliflower) Rice Blend (sold by the pound), UPC #253162000000
The recalled products were distributed to 98 Wegmans stores in N.Y., N.J., Pa., Md., Va. and Mass.
No illnesses have been reported to date.
The recall was initiated by Produce Packaging, Inc. based in Cleveland, OH, which supplies these products to Wegmans and notified Wegmans that the product may have been contaminated.
Wegmans has placed automated phone calls to customers who purchased the product using their Shoppers Club card.
Customers who purchased the recalled products from Wegmans between December 7 and December 18 should return them to the service desk for a full refund. Consumers with questions may contact Wegmans Consumer Affairs department toll free at 1-855-934-3663 Monday through Friday, between 8:00 a.m. and 5:00 p.m. Eastern time. - Jennie-O Turkey Store Sales, Inc., a Faribault, Minn. establishment, is recalling approximately 164,210 pounds of raw ground turkey products that may be contaminated with Salmonella Reading, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw ground turkey items were produced on October 22, 2018 and October 23, 2018. The following products are subject to recall: [View Labels (PDF only)]
3-lb. packages of “Jennie-O GROUND TURKEY 93% LEAN | 7% FAT” with “Use or freeze by” dates of 11/12/18 and 11/13/18 on the side of the trays.
1-lb. packages of “Jennie-O GROUND TURKEY 93% LEAN | 7% FAT” with “Use or freeze by” dates of 11/12/18 on the side of the trays.
1-lb. packages of “Jennie-O TACO SEASONED GROUND TURKEY” with “Use or freeze by” dates of 11/12/18 on the side of the trays.
1-lb. packages of “Jennie-O ITALIAN SEASONED GROUND TURKEY” with “Use or freeze by” dates of 11/12/18 on the side of the trays.
3-lb. packages of “Jennie-O Ground Turkey 85% LEAN | 15% FAT” with a “Use or freeze by” date of 11/13/18 on the side of the trays.
2.5-lb. packages of “Jennie-O Ground Turkey 93% LEAN | 7% FAT” with a “Use or freeze by” date of 11/13/18 on the side of the trays.
3-lb. packages of “STATER BROS. 85% LEAN | 15% FAT ALL NATURAL Ground Turkey” with a “Use or freeze by” date of 11/12/18 on the side of the trays.Consumers with questions regarding the recall can contact Hormel Consumer Engagement, at (800) 621-3505. Media with questions regarding the recall can contact Media Relations at, media@hormel.com or (507) 434 6352. - RXBAR has recalled the following products with the specified date codes, as these products may contain traces of peanuts, which are not listed in the ingredients:
RXBAR Description UPC Number BEST BY Date Code
Chocolate Sea Salt 8-57777-00423-2 06 10 2019 through 06 15 2019
Coconut Chocolate 8-57777-00421-8 06 15 2019 through 06 17 2019 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] - Inspired Organics, LLC has issued a voluntary recall of Organic Almond Butter due to potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The product was distributed exclusively by Lipari Foods. LLC in Warren, Michigan to food service and retail stores throughout Florida, Illinois, Indiana, Kentucky, Michigan, Minnesota, Missouri, Ohio, Pennsylvania, Tennessee, West Virginia, and Wisconsin.
The affected product can be identified by:
Brand
Product
Lipari Item #
Size
Best By Date
Lot #
UPC
Inspired Organics
Organic Almond Butter
967067
16oz
02/20
239
863669742540
This was brought to our attention after product testing initiated by Inspired Organics LLC returned positive test results for Listeria monocytogenes contamination. Inspired Organics initiated this testing out of an abundance of caution following a previous recall of a similar product which had also tested positive for contamination of Listeria monocytogenes through testing conducted by the Michigan Department of Agriculture and Rural Development (MDARD). We are working closely with the manufacturer, MDARD, and the Food and Drug Administration (FDA) to understand the cause of the situation and ensure that all affected product has been pulled from commerce. No illnesses have been reported to date.
Lipari Foods began shipping the product on October 31, 2018.
Consumers who have purchased these recalled products should not consume them. Consumers should discard the products or return them to the point of purchase. Consumers with questions should call Customer Service at 800-729-3354, 8:15 am – 4:30 pm, EST, Monday through Friday.
Link to Original Recall - Russ Davis Wholesale, Inc., a Pueblo, Colo. establishment, is recalling approximately 956 pounds of ready-to-eat poultry 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 eggs, a known allergen, which is not declared on the product label.
The ready-to-eat chicken Caesar wrap items were produced on various dates from Nov. 12, 2018 through Dec. 16, 2018. The following product is subject to recall: [View Labels (PDF only)]
11.3-oz. plastic clamshell packages containing “Boar’s Head EVERROAST CHICKEN CAESAR WRAP,” with “SELL BY” dates from 11/15/18 through 12/19/18.
The product subject to recall bears establishment number “P45204B” inside the USDA mark of inspection. These items were shipped to retail locations in New Mexico.
The problem was discovered on Dec. 17, 2018 when the company notified FSIS inspection program personnel that the incorrect ingredient statement had been used for the final product.
There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider. Members of the media with questions about the recall can contact Amy Rotenberg at (202) 756-1028. Consumers with questions about the recall can contact Russ Davis Wholesale, Inc. Customer Service at (877) 433-2173. - Adam Bros. Farming, Inc. of Santa Maria, California is recalling red leaf lettuce, green leaf lettuce and cauliflower harvested on November 27 through 30, 2018 out of an abundance of caution, because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7).
None of the recalled product has tested positive for E. coli O157:H7. No illnesses have been reported.
Adam Bros. Farming, Inc. feels a strong commitment to its customers and has worked for years to provide a safe and healthy food supply. Out of an abundance of caution, Adam Bros.
Farming, Inc. is initiating this voluntary recall in cooperation with the FDA. The recall involves produce harvested between November 27, 2018 and November 30, 2018, grown in particular fields. It does not involve all of Adam Bros. Farming, Inc.’s products. As of 12/13/2018 Adam Bros. Farming, Inc. has notified its effected customers of all product that was recalled, asking that the product not be eaten, sold, or transferred. Furthermore, Adam Bros. Farming, Inc. asked that its customers notify the downline chain of custody to insure a full recall.
Cauliflower was distributed to wholesalers in AZ, CA, IL, LA, MD, NC, NJ, NY, OH, PA. Tijuana, Mexico, and Canada ; red and green leaf lettuce was distributed to wholesalers in CA, CO, OR, TX, PA, WA, and Canada; red leaf lettuce only was distributed to a wholesaler in MN, and Tijuana, Mexico.The recall was initiated after it was discovered that sediment from a reservoir near where the produce was grown tested positive for E. coli O157:H7. Filtered and treated water from the reservoir may have come in contact with the produce after it was harvested. None of the filtered, treated water has tested positive for E. coli, all E. coli tests returning negative. This bacteria may cause a diarrheal illness from which most healthy adults can recover completely within a week. Some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death.Consumers who have purchased any of the referenced product are urged to return it to the place of purchase or destroy it. Consumers with questions may contact the company at 1-805-925- 0339 - Russ Davis Wholesale, Inc., a Pueblo, Colo. establishment, is recalling approximately 956 pounds of ready-to-eat poultry 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 eggs, a known allergen, which is not declared on the product label.
The ready-to-eat chicken Caesar wrap items were produced on various dates from Nov. 12, 2018 through Dec. 16, 2018. The following product is subject to recall: [View Labels (PDF only)]
11.3-oz. plastic clamshell packages containing “Boar’s Head EVERROAST CHICKEN CAESAR WRAP,” with “SELL BY” dates from 11/15/18 through 12/19/18.
The product subject to recall bears establishment number “P45204B” inside the USDA mark of inspection. These items were shipped to retail locations in New Mexico.There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider. Members of the media with questions about the recall can contact Amy Rotenberg at (202) 756-1028. Consumers with questions about the recall can contact Russ Davis Wholesale, Inc. Customer Service at (877) 433-2173. - Kimberly-Clark announced a voluntary product recall of its U by Kotex® Sleek® Tampons, Regular Absorbency, sold throughout the United States and Canada for a quality-related defect that could impact the performance of this product.
The recall is limited to specific lots of U by Kotex® Sleek® Tampons, Regular Absorbency, that were manufactured between October 7, 2016 and October 16, 2018 and distributed between October 17, 2016 and October 23, 2018. Consumers can identify this product by looking for specific lot numbers found on the bottom of the package. A full list of recalled lot numbers is available on the U by Kotex® website. Retailers have been alerted to remove the recalled lot numbers from shelves and post a notification in their stores.
No other U by Kotex-branded products are subject to this recall.
Kimberly-Clark has received reports from consumers of the U by Kotex® Sleek® Tampons, Regular Absorbency, unraveling and/or coming apart upon removal, and in some cases causing users to seek medical attention to remove tampon pieces left in the body. There also have been a small number of reports of infections, vaginal irritation, localized vaginal injury, and other symptoms.
Any consumer with the impacted U by Kotex® Sleek® Tampons, Regular Absorbency, in their possession should stop using the product immediately and promptly contact Kimberly-Clark’s Consumer Service team at 1-888-255-3499 between 7:30 a.m. – 7:00 p.m. Central Time, Monday through Friday, for information regarding this recall. Consumers who experience vaginal injury, (pain, bleeding, or discomfort), vaginal irritation (itching or swelling), urogenital infections (bladder and/or vaginal bacterial and/or yeast infections), or other symptoms such as hot flashes, abdominal pain, nausea, or vomiting following use of the impacted product should seek immediate medical attention. http://www.kimberly-clark.com/ - Mannarich Food, Inc., the Importer of Record, a Toronto, Canada firm, is recalling approximately 145,245 pounds of Siluriformes products that were not presented at the U.S. point of entry for inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The Siluriformes products were imported to the U.S. on various dates from June 26, 2017 through November 13, 2018. The products have a shelf life of two years and all lots produced are included in the recall. The following products are subject to recall:
300-g. plastic containers containing “FISH PASTE.”
300-g. plastic containers containing “MANNARICH FISH PASTE WITH BLACK MOSS.”
2-kg. sealed plastic bags containing “FISH PASTE WITH BLACK MOSS.”
3-kg. sealed plastic bags containing “FISH BALL WITH BLACK MOSS.”
2-kg. sealed plastic bags containing “FISH PASTE.”
The products were imported from Malaysia, a country that is not eligible to export Siluriformes to the United States. These items were shipped to a wholesale and retail locations nationwide.Consumers and members of the media with questions about the recall can contact Raphael Lo, Operations Manager of Mannarich Foods, Inc. at (647) 228-0204. - Achdut LTD. of Ariel, Israel, is recalling its Tahini products of all packages and sizes produced on the following dates: April 7th to May 21st 2018, because it may 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 “Tahini” was distributed internationally in retail stores and through mail orders.
The tahini products are Tahini, Whole Tahini, Organic Tahini and Seasoned Tahini. Container sizes: 15oz, 16oz, 17.6oz, 635 oz (428g, 454g, 500g, 18Kg), with lot numbers 18-097 to 18-141 or with expiration dates April 7th to May 21st 2020, while the Baron’s brand carries an expiration date of 5/5/2021. The brand names of the products are: Achdut, Baron’s, S&F, Pepperwood, Soom and Achva.
Achdut is collaborating with health officials in connection with a positive finding of Salmonella in a US import sample of Achdut Tahini linked to a Salmonella outbreak that is currently being investigated by FDA and public health officials.
The probable root cause for this recall is cross contamination. The company has eliminated the source of contamination and preventive steps were taken.
Consumers who have purchased the Tahini above are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 972-3-9068020, Sun-Thu 08:00-17:00 GMT+2. - Vermont Packinghouse, LLC, a N. Springfield, Vt. establishment, is recalling approximately 10,828 pounds of raw intact bone-in beef quarters from cattle identified as being over 30 months of age because the products may contain specified risk materials (SRM), specifically vertebral column, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The carcasses were slaughtered from Feb. 8, 2018 to June 8, 2018. The following products are subject to recall:
White butcher paper wrapped packages of fresh T-bone and Porterhouse steaks from Walden Local Butcher Shop in Boston, Massachusetts.
The quartered carcasses were shipped from Vermont Packinghouse, LLC to the one retail location for further processing and were wrapped in butcher paper for consumers. The products were only sold at the one physical retail location. The products were not shipped to consumers who have memberships with the retailer. - Amboy Group, LLC, a Woodbridge, N.J. establishment, is recalling an undetermined amount of raw boneless and skinless poultry products because the products are misbranded and may contain milk, egg, and soy, known allergens, which are not declared on the finished product label, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw boneless and skinless poultry products were produced on various dates from Dec. 5, 2016 through Dec. 5, 2018. The following products are subject to recall: [View Labels (PDF Only)]
16-oz. plastic trays of “Shop Rite Ready To Cook BONELESS & SKINLESS Chicken Breast Italian Style Panko Breaded.”
16-oz. plastic trays of “Shop Rite Ready To Cook BONELESS & SKINLESS Chicken Breast Sundried Tomato Panko Breaded.”
16-oz. plastic trays of “Shop Rite Ready To Cook BONELESS & SKINLESS Chicken Breast Parmesan Panko Breaded.”
16-oz. plastic trays of “Shop Rite Ready To Cook BONELESS & SKINLESS Chicken Breast Mustard Panko Breaded.”
The products subject to recall bear establishment number “EST. P-33789” inside the USDA mark of inspection. These items were shipped to retail locations in New Jersey. Consumers and members of the media with questions about the recall can contact Logan McNamara, Controller of Amboy Group, LLC, at (732) 682-8329. - Vermont Packinghouse, LLC, a N. Springfield, Vt. establishment, is recalling approximately 10,828 pounds of raw intact bone-in beef quarters from cattle identified as being over 30 months of age because the products may contain specified risk materials (SRM), specifically vertebral column, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The carcasses were slaughtered from Feb. 8, 2018 to June 8, 2018. The following products are subject to recall:
White butcher paper wrapped packages of fresh T-bone and Porterhouse steaks from Walden Local Butcher Shop in Boston, Massachusetts.
The quartered carcasses were shipped from Vermont Packinghouse, LLC to the one retail location for further processing and were wrapped in butcher paper for consumers.Consumers and media with questions about the recall can contact at Arion Thiboumery, General Manager of Vermont Packinghouse, LLC, at (802) 886-8688 ext. 2001. - CTI Foods LLC, an Owingsville, Ky. establishment, is recalling approximately 29,028 pounds of frozen, ready-to-eat (RTE) pork and poultry sausage links products that may be contaminated with extraneous materials, specifically pieces of metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The frozen, ready-to-eat sausage links items were produced and packaged on Aug. 4, 2018. The following products are subject to recall: [View Label (PDF Only)]
23.4-oz. pouches of “Jimmy Dean HEAT ’n SERVE Original SAUSAGE LINKS Made with Pork & Turkey” with a Use By date of Jan. 31, 19. The product bears case code A6382168, with a time stamp range of 11:58 through 01:49.
The products subject to recall bear establishment number “EST. 19085” on the back of the product packaging. These items were shipped to an establishment in Tennessee where the product was further distributed to retail stores.
The problem was discovered on Dec. 10, 2018, when FSIS received notification that the establishment had received five consumer complaints of metal pieces in the RTE sausage links.
Consumers with questions about the recall can contact the Jimmy Dean customer service line at (855) 382-3101. Members of the media with questions about the recall can contact Worth Sparkman, senior manager for communication, at (479) 290-6358. - • 085-2018 Expansion, JBS Tolleson, Inc. Recalls Raw Beef Products Due to Possible Salmonella Newport Contamination (Dec. 4, 2018)
• 085-2018, JBS Tolleson, Inc. Recalls Raw Beef Products Due to Possible Salmonella Newport Contamination (Oct. 4, 2018) - Tris Pharma, Inc. has voluntarily recalled three (3) lots of Infants’ Ibuprofen Concentrated Oral Suspension, USP (NSAID) 50 mg per 1.25 mL, to the retail level. The recalled lots of the product have been found to potentially have higher concentrations of ibuprofen.The product is used as a pain reliever/fever reducer and was packaged in 0.5 oz. bottles for the recalled lots listed below:
NDC;
LOT;
EXPIRATION;
DESCRIPTION ;
COMPANY;
49035-125-23
00717009A
00717015A
00717024A
02/19
04/19
08/19
Equate: Infants’ Ibuprofen Concentrated Oral Suspension,
USP (NSAID), 50 mg per 1.25 mL,
0.5 oz. bottle
Wal-Mart Stores Inc
59779-925-23
00717024A
08/19
CVS Health: Infants’ Ibuprofen Concentrated Oral Suspension,
USP (NSAID), 50 mg per 1.25 mL,
0.5 oz. bottle
CVS Pharmacy
55319-250-23
00717024A
08/19
Family Wellness: Infants’ Ibuprofen Concentrated Oral Suspension,
USP (NSAID), 50 mg per 1.25 mL,
0.5 oz. bottle
Family Dollar Services Inc.
Tris Pharma, Inc. sold the affected lots of Ibuprofen Concentrated Oral Suspension, USP (NSAID) 50 mg per 1.25 mL to one customer, which distributed the lots into the US market. Tris Pharma, Inc. has notified its customer by urgent recall notice and is arranging for the return of the recalled product.
Wholesalers and retailers of the product should stop further distribution of the affected lots of Ibuprofen Concentrated Oral Suspension, USP (NSAID) 50 mg per 1.25 mL, which are being recalled.
Consumers with questions regarding this recall can contact Tris Customer Service at 732-940-0358 (Monday through Friday, 8:00am ET- 5:00pm PT) or via email at Customer Service Email . 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.
- JBS Tollseon Updates go to: foodsafetynews.com
- JBS Tolleson, Inc., a Tolleson, Ariz. establishment, is recalling approximately 12,093,271 pounds of non-intact raw beef products that may be contaminated with Salmonella Newport, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The raw, non-intact beef items, including ground beef, were packaged on various dates from July 26, 2018 to Sept. 7, 2018. The following products are subject to recall: [Products List (PDF) | Product Labels (PDF only)| The products subject to recall bear establishment number “EST. 267” inside the USDA mark of inspection. These items were shipped to a retail locations and institutions nationwide. AfterFSIS Recall 085-2018 on October 4, 2018, FSIS, CDC, and state public health and agriculture partners continued to investigate the outbreak of Salmonella Newport illnesses. The epidemiological investigation has identified 246 confirmed case-patients from 26 states with illness onset dates ranging from July 26 to September 7, 2018. An additional 16 case-patients have provided receipts or shopper card numbers for the product traceback investigations. Specific traceback for three case-patients have identified JBS Tolleson, Inc., EST. 267 ground beef products that were not part of the October 4, 2018 recall. FSIS will continue to work with public health partners and provide updated information should it become available. Consumers with questions regarding the recall can contact the JBS USA Consumer Hotline at (800) 727-2333. Members of the media with questions regarding the recall can contact Misty Barnes, public relations specialist at JBS USA, at (970) 506-7805.
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