Glenmark's Ziac blood pressure tablets contaminated with cholesterol drug ezetimibe prompts FDA recall affecting multiple ...

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

Neither the FDA nor Glenmark Pharmaceuticals have issued guidance for consumers who may have the medication involved in this ...

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

The FDA rarely uses its authority to pull dangerous medical devices off the market and is so poorly staffed that it's ...

A voluntary, nationwide recall has been issued for a common ADHD medication, lisdexamfetamine dimesylate The U.S. Food and Drug Administration has designated this a Class II recall, meaning it is ...

The Food and Drug Administration has recalled a popular treatment for high blood pressure. The agency said that bottles of bisoprolol fumarate and hydrochlorothiazide tablets, under the brand name ...

Since the start of the month, several drug recalls have entered the FDA’s periphery, affecting products ranging from hospital drugs and potassium deficiency ...

The U.S. Food and Drug Administration is recalling 41,328 bottles of Walgreens Saline Nasal Spray with Xylitol due to the presence of a bacteria commonly found in raw milk, according to the FDA. READ ...

The FDA says four major retailers including Walmart, Target, Kroger and Albertsons continued to sell ByHeart baby formula ...

The Illinois lawmakers want an electronic format for medical device makers to quickly and transparently report recall information to federal regulators.

The FDA’s oversight of medical device recalls continues to be plagued by staffing challenges—forcing some activities to be ...