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Mondelēz Global announced a recall for various sizes of Ritz peanut butter cracker sandwiches over possible undeclared ...
The FDA's assessment of the bread recall has designated it as a Class II risk, which means the product "may cause temporary ...
13h
Explícame on MSNFDA Orders Recall of Ritz Cracker Sandwiches Due to Allergy Risk, Sold at Costco, Walmart, Target, and More
The FDA has announced a nationwide recall of Ritz Cracker Sandwiches due to undeclared peanut allergens. Initiated by Mondelez Global LLC, this voluntary action affects products sold at major ...
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MiBolsilloColombia on MSNHighest risk warning from FDA on chocolate recall; Check if you're affected
The FDA has issued Class I recalls for chocolate products due to undeclared allergens and contamination—posing serious health ...
The FDA today issued a notice warning of a recall of arterial perfusion cannula devices made by Edwards Lifesciences (NYSE:EW ...
Lupin Pharmaceuticals’ Clomipramine Hydrochloride capsules are used “for the treatment of obsessions and compulsions in patients with Obsessive-Compulsive Disorder (OCD),” according to the National ...
(FDA / Fox News) The reclassification did not state any illnesses or deaths related to the recall. A view of the back of a bag of the impacted shelled walnuts, with UPC Code 7 15001 00908 1.
Recalls And Warnings ‘May contain metal pieces’: FDA updates recall for granola bars sold nationwide by: Emily Smith, Laura Morrison. Posted: Feb 17, 2025 / 03:11 PM EST.
Thousands of cases of ice cream sold nationwide, including New York state, are being recalled for potential bacteria contamination. The U.S. Food & Drug Administration recently updated its risk ...
The Food and Drug Administration has issued warning letters to three makers of infant formula — ByHeart Inc., Reckitt/Mead Johnson Nutrition, and Perrigo Wisconsin, LLC — after finding ...
The FDA is hoping to avoid a repeat of the "large-scale" baby formula recall that took place in late 2022 and early 2023 and contributed to a shortage, Prater said.
In the new warning letter sent to Perrigo, the FDA details that Cronobacter had been identified in finished formula products on multiple occasions by the company: in two products "during a ...
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