In the news

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In Canada, microgreens, a potent mix prepared and sold by the company Micro plants Robert recalled its product due to generic E. coli

The Ministry of Agriculture, Fisheries and Food (MAPAQ), in collaboration with the company Micro plants Robert (911, Rue Principale, in Batiscan), is advising the public not to consume the Microgreen full-bodied mix in a 60 g package due to generic E. coli bacteria (non-pathogenic serotype). The product was offered for sale in several establishments in Quebec. The product was packaged in a clear plastic container. It was sold refrigerated. It has been agreed upon with MAPAQ that this warning should be issued as a precautionary measure. @ https://www.quebec.ca/nouvelles/actualites/details/avis-de-ne-pas-consommer-de-micro-pousses-melange-corse-prepare-et-vendu-par-lentreprise-micro-plants-robert-61743

 

MISE EN GARDE À LA POPULATION QUÉBEC, le 22 mars 2025 /CNW/ – Le ministère de l’Agriculture, des Pêcheries et de l’Alimentation (MAPAQ), en collaboration avec l’entreprise Micro plants Robert, située au 911, Rue Principale, à Batiscan, avise la…

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The CORE update of March 27, 2025

The CORE update list of outbreaks and adverse events includes four entries. The outbreak of Listeria monocytogenes (ref #1286) linked to an unidentified product, the case count has increased from 28 to 30. The outbreak of Salmonella Newport (ref #1291) linked to an unidentified product, the case count was adjusted to 35 to include cases that were reported after the outbreak was declared over. The FDA’s investigation of the outbreak of Listeria monocytogenes (ref # 1285) has closed. @ 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 USDA Food recalled for 2012-2023 compared with FDA Regulated food recalls over the past two decades

An article entitled “USDA Food Recalls for the period 2012-2023 compared with FDA Regulated Food Recalls over the past two decades” was published in JFP. This manuscript evaluates recalls of food products regulated by the USDA/ FSIS. The FSIS regulates food products made from animals raised on farms, including beef, pork, poultry, buffalo, and venison, as well as some egg products and farmed or wild-caught seafood of the order of Siluriformes (catfish). During the 12 years of 2012-2023, 1,001 food recall incidents occurred, representing 205.2 million lbs of recalled product. The FSIS classified these recall incidents at 76% as Class I, 20% as Class II, and 4% as Class III. The causes of the recalls were combined for this analysis into three master categories: Product Contaminants, Processing Issues, and Other Reasons. Product Contaminants caused 68% of the FSIS recalls, Processing Issues added 13%, and Other Reasons contributed 19%. Further evaluation of these recall incidents by product type resulted in poultry at 29%, beef at 23%, Mixed Animal meat at 23%, and pork at 22% of the recall incidents. Evaluation of these recalls by product weight showed Mixed Animal meat at 52%, Poultry at 27%, Beef at 16%, and Pork at 4%. Biological Contamination was a component of the product contaminants master category, and 4 bacterial species caused almost 59% of the FSIS recalls by weight. Listeria monocytogenes caused 32%, Shiga toxin-producing E. coli (STEC) caused 12%, Salmonella serovars caused 9%, and Bacillus cereus caused 0.5% of these recalls by weight. These FSIS food recalls were compared to the FDA Food & Beverage recalls from a recent publication. Listeria was the common cause of the highest percentage of FDA recalled by incidents, and FSIS recalls by weight. Most of the food recalls were caused by human error. Developing a strong Food Safety Culture along with strong cleanup and sanitation procedures is imperative to minimizing and preventing food recalls. @ https://pdf.sciencedirectassets.com/782803/AIP/

 

 

 

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In the News January 2025-June 2025 FDA advises restaurants, retailers, and consumers not to serve, sell, or eat frozen half-shell oysters from the Republic of Korea due to Norovirus

The FDA updated the Safety Alert after a recall was issued by Daihung Mulsan Co., Ltd. (KR 7 SP) of the Republic of Korea (ROK) to include additional harvest dates of certain frozen half shell oysters because they may be contaminated with Norovirus. The voluntary recall includes additional oysters that were processed by KR-7-SP in ROK and harvested from Designated Area II on the following dates: 01/31/2024, 02/01/2024, and 02/02/2024, as well as those identified in the initial recall of 01/30/2025 and 02/04/2025. The oysters were shipped to Sea Win, Inc. of Los Angeles, CA, and may have been further distributed. The product was recalled by the importer, Sea Win, Inc. (CA 353 SS) of Los Angeles, CA, on 3/7/2025. The FDA is advising restaurants and food retailers not to serve or sell and to dispose of, and consumers not to eat, these frozen half-shell oysters because they may be contaminated with Norovirus @ https://www.fda.gov/food/alerts-advisories-safety-information/fda-advises-restaurants-and-retailers-not-serve-or-sell-and-consumers-not-eat-certain-frozen-half?utm_medium=email&utm_source=govdelivery

 

Safety Alert

Sea Win (CA 353 SS) of Los Angeles, CA has recalled frozen half-shell oysters from KR-7-SP, harvested on 1/30/2024 and 2/4/2024 from Designated Area II in the ROK due to an outbreak of norovirus illnesses.