Big retailers didn’t pull ByHeart baby formula fast enough after botulism recall, FDA says

The U.S. Food and Drug Administration sent warning letters to four top retail stores for failing to promptly pull ...

FDA sends warning letters to major retailers for selling recalled formula linked to infant botulism outbreak

The US Food and Drug Administration sent warning letters to Target, Walmart, Kroger and Albertsons after some of the stores ...

FDA sends warning letters to Walmart, Target for selling recalled baby formula

Four major retailers kept ByHeart infant formula on store shelves even after being notified of the recall, the FDA said. The ...

FDA says retailers didn't remove recalled formula fast enough

More than 50 infants in 19 states have been hospitalized due to the outbreak.

FDA warns Target, Walmart, Kroger and Albertsons after recalled ByHeart formula stayed on shelves

The FDA said it would take steps to improve its recall enforcement after four of the nation's largest retail stores failed to ...

Walmart, Target, Kroger failed to remove recalled baby formula linked to ‘potentially fatal’ illness: FDA

Federal regulators slapped four of the nation’s biggest retailers with warning letters after investigators found recalled ...
The Virgin Islands Consortium

Teva Recalls Blood Pressure Drug Over Elevated Cancer-Linked Impurity

Teva Pharmaceuticals USA has issued a nationwide recall of hundreds of thousands of bottles of a commonly prescribed blood ...

Nut recall in 10 states as FDA issues warning

Mellace issued a recall for two types of ‘Wegmans Deluxe Mixed Nuts Unsalted’ sold at Wegmans stores.
Health

FDA Announces Nationwide Recall of Common Blood Pressure Medication—More Than 11,000 Bottles Affected

A generic version of Ziac, made by Glenmark Pharmaceuticals, may be contaminated with trace amounts of a cholesterol ...
MedTech Dive

FDA needs more staff, authority to oversee device recalls, watchdog finds

FDA's challenges — such as insufficient staffing — can create inefficiencies in the process and potentially put lives at risk ...

Urgent recall: Factory error puts wrong drug in blood pressure meds

The Food and Drug Administration (FDA) classified the recall with a Class lll risk level, suggesting that exposure to the ...

The FDA Rarely Forces Manufacturers to Recall Dangerous Medical Devices, Watchdog Report Finds

Lawmakers requested the report after a 2023 ProPublica and Pittsburgh Post-Gazette investigation revealed that the FDA had ...