The CFIA reported that CLS Catering Services Ltd. recalled “Fresh and Local” brand turkey and bacon sub sandwiches from the marketplace due to Listeria monocytogenes. The company triggered the recall. The recalled product has been sold in British Columbia. There have been no reported illnesses associated with the consumption of this product. @ https://recalls-rappels.canada.ca/en/alert-recall/fresh-and-local-brand-turkey-bacon-sub-recalled-due-listeria-monocytogenes?utm_source=gc-notify&utm_medium=email&utm_content=en&utm_campaign=hc-sc-rsa-22-23&
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The FDA team updated the CORE table: Traceback has been initiated for the Listeria monocytogenes outbreak (ref# 1106) in a not yet identified product. For the Salmonella Mississippi outbreak (ref# 1097) in a not yet identified product, the case count changed from 102 to 103. For the Salmonella Senftenberg outbreak (ref# 1087) in a not yet identified product, the case count changed from 27 to 30. For the Salmonella Typhimurium outbreak (ref# 1095) in a not yet identified product, the case count changed from 78 to 84. For the Cyclospora outbreak (ref# 1080) in a not yet identified product, the case count changed from 79 to 81. All the foods on the list are yet unidentified. @ https://www.fda.gov/food/outbreaks-foodborne-illness/investigations-foodborne-illness-outbreaks?utm_medium=email&utm_source=govdelivery
The following is a list of outbreak and adverse event investigations primarily being managed by FDA’s CORE Response Teams.
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The CFIA reported that Kam Ding Investment Ltd had recalled K-fresh produce brand from the Canadian market due to potential contamination with Listeria monocytogenes. Canadian Food Inspection Agency test results triggered the recall. There have been no reported illnesses associated with the consumption of this product. The recalled Enoki has been sold in British Columbia and may have been distributed in other provinces and territories. @ https://recalls-rappels.canada.ca/en/alert-recall/k-fresh-fresh-produce-brand-enoki-mushroom-recalled-due-listeria-monocytogenes?utm_source=gc-notify&utm_medium=email&utm_content=en&utm_campaign=hc-sc-rsa-22-23&
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The FDA reported that Family Dollar recalled products that were stored and inadvertently shipped to certain stores on or around May 1, 2022, through June 10, 2022, due to products being stored outside of labeled temperature requirements. This notice covers the recall of Over-the-Counter Medical Devices. An earlier notice issued on July 21, 2022, covered a related recall of Over-the-Counter Pharmaceutical Products. To date, Family Dollar has not received any consumer complaints or reports of illness related to this recall. A list of the recalled products is attached. This recall goes to the retail store level. Not all of the products listed were sent to all stores. This recall does not apply to Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont, Washington, Alaska, or Hawaii. Because Family Dollar does not have any stores in Alaska or Hawaii and no Family Dollar stores in any of the other states received any products subject to this recall. @ https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-certain-over-counter-products-sold-family-dollar-stores-because-they-were-stored?utm_medium=email&utm_source=govdelivery
Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being stored outside of labeled