Woman's World on MSN6d
Milk Recall: 20,000 Cases Removed Due to Premature Product Spoilage
If you prefer cow’s milk to non-dairy options and regularly pick up some at the grocery store, you may want to be extra ...
FDA Recalls Blood Pressure Drug Over ‘Visible Black’ Contaminants
Medicine may not be an exact science, but precision is crucial for patient care. That’s why the presence of unknown particles ...
Lay’s Potato Chip Recall Increased to Highest Risk Level, FDA Warns Product Could Cause 'Death’
Lay’s voluntary recall from December has been increased to the U.S. Food and Drug Administration’s highest risk level ...
Nationwide Blood Pressure Drug Recall As FDA Issues Fatal Warning
An injectable blood pressure drug has been recalled after the FDA has warned it could cause side effects, such as stroke or death.
Frito Lay's Classic Potato Chips: Recall raised to highest risk level by FDA. What to know
The specifically recalled chips were: 13-ounce bags of Lay's Classic Potato Chips with UPC of 28400 31041, a "Guaranteed ...
The Healthy on MSN11h
More Than 160,000 Lots of a Drug for Men Recalled in 30 States and Internationally
Walmart, CVS, Amazon and other well known retailers may have carried the recalled product, which the FDA calls out unique ...
MLive1h
This chocolate recall has been upgraded to FDA’s highest risk level
STATEN ISLAND, N.Y. — A December 2024 chocolate recall has been upgraded to highest risk level by the U.S. Food and Drug ...
Pet food, raisins, and pancake mix among FDA recall list for January 2025
It's a new year, which means several new food items were deemed unsafe due to recalls by the U.S. Food and Drug Administration.
MLive13h
Lay’s potato chip recall now elevated to FDA’s highest-risk level
The FDA has upgraded a recall of Lay’s Potato Chips to the highest level possible, meaning consuming the chips will cause ...
FDA elevates Lay's potato chip recall in Oregon, Washington to highest risk level
Class I, according to the FDA, means exposure to or consumption of the product could cause "serious adverse health ...
Sunscreen Recalled Nationwide as FDA Sets Risk Level
A voluntary recall was initiated by The W.S. Badger Company due to missing labels on a sunscreen product distributed nationwide.
ConsumerAffairs3d
Drug used to treat low blood pressure recalled
Provepharm is recalling lot number 24020027; Expiry Date December 2025 of Phenylephrine hydrochloride Injection, USP, 10 mg/ ...