A daily medication relied on by more than half a million women is under urgent recall after a critical test failure raised ...

The recall will remain active until the FDA and Carley's Inc. have resolved the labeling issue and ensured that all ...

One lot of reflux medicine got recalled when fluid retention tablets were discovered in the medicine bottles.

A Class I recall is reserved for products that pose a serious health risk with a "reasonable probability" of causing illness or even death if consumed. The recalled Greek salads were sold under ...

A Mahwah-based drugmaker is being sued after recalling millions of potassium chloride capsules linked to serious health risks ...

Provepharm is recalling lot number 24020027; Expiry Date December 2025 of Phenylephrine hydrochloride Injection, USP, 10 mg/ mL at the hospital/institutional level. This recall was initiated based ...

It's an evolved (and less prickly way) to monitor blood glucose, but a well known brand's defect could result in serious ...

The FDA is assigning the drug duloxetine delayed-release capsules to the second-highest risk level after drug distribution company, Breckenridge Pharmaceutical Inc., voluntarily issued the recall ...

A recall of Lay’s potato chips was upgraded this week to the Food and Drug Administration’s most-severe level.. The agency on Monday assigned a Class I recall to 6,344 bags of Lay’s Classic ...

The recall level has been elevated to the highest the U.S. Food & Drug Administration (FDA) has, meaning the broccoli may potentially be deadly to susceptible individuals.

Aurobindo also recalled an undisclosed amount of nebivolol 2.5 mg tablets in 30-count bottles due to the presence of excess levels of the nitrosamine drug substance-related impurity N-Nitroso ...