FDA issues highest alert for cheese due to listeria risk – NewsNation NewsNation The FDA has issued the highest alert for a cheese recall for concerns over listeria contamination.
FDA Issues Recall for Potentially Radioactive Shrimp – Newser Newser The FDA says roughly 83,800 bags of frozen raw shrimp imported from … This is the latest of 12 notices in the FDA’srecall of potentially radioactive …
FDA announces recalls of sweet treats 2 days before Christmas – NewsNation NewsNation Silvestri Sweets Inc. of Geneva, Illinois, is expanding its recall of Choceur-branded Holiday Barks over multiple undeclared allergens. Recalled …
Brand of chocolate bar recalled by FDA due to undisclosed almonds – Austin American-Statesman Austin American-Statesman The FDA has recalled Willy Pete’s chocolate bars after discovering almonds were not listed on the ingredient label, raising allergy concerns.
Aldi has expanded on a previous recall for its chocolate holiday bark to include more lot numbers and best-by dates than originally announced, according to the U.S. Food & Drug Administration (FDA). The grocery store is recalling even more bags of its Choceur-branded Cookie Butter Holiday Bark and Choceur-branded Pecan, Cranberry & Cinnamon Holiday Bark due to a packaging error that left the Cookie Butter-flavored bark in the Pecan, Cranberry & Cinnamon-flavored bark bag, and vice versa. Therefore, neither packages contain the proper allergen warnings.
Olympia Provisions of Portland, Ore., is recalling approximately 1,930 pounds of its ready-to-eat holiday kielbasa sausages because the product may be contaminated with foreign material, specifically metal, according to the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS). Read More –
FDA expands nationwide recall of nasal sprays – YouTube YouTube Authorities said the products may contain yeast, mold, or other microbial contamination above acceptable levels.
FDA confirms new recall for Johnson & Johnson heart device over safety concerns Cardiovascular Business Three patient deaths have been linked to connectivity issues with these devices. The FDA has classified this as a Class I recall.
