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

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

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

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

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 ...

Nearly 300,000 bottles of the drug, named Cinacalcet, were recalled and given a Class II recall risk level by the FDA. Nearly 300,000 bottles of the drug, named Cinacalcet, ...

The U.S. Food and Drug Administration updated the risk level of an antidepressant recall to the second-highest level due to the product containing high levels of a cancer-causing chemical.

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.