Prestige Consumer Healthcare Inc. issued a voluntary recall for more than 10,000 cases of honey cough syrup on June 17.

White House officials overrode NIH career staff in deciding which "dangerous gain-of-function research" projects on viruses ...

FDA recalls Dexcom glucose monitors (G6, G7, ONE models) due to alert issues posing severe health risks. Read more here.

The Food and Drug Administration July 15 announced a recall by Sandoz on certain lots of cefazolin, due to the lots being ...

Consumers who have purchased the affected product should not consume it, per the FDA. For information on refunds (or for more ...

More than 67,000 cases of Power Stick deodorant were recalled over manufacturing defects, according to the FDA.

More than 67,000 cases of a popular deodorant brand sold by retailers nationwide were recalled due to an undisclosed ...

The Food and Drug Administration has announced the recall of two types of sprouted beans because they may be contaminated ...

The Food and Drug Administration (FDA) has issued a recall involving tens of thousands of Power Stick antiperspirant ...

As such, the FDA has classified the New Mexico Pinon Coffee pod recall as a Class III risk. The FDA defines such a risk as “a ...

The defect has resulted in problems including a procedural delay, difficulty removing device fragments and bleeding, the FDA ...

The FDA announced the recall of nearly 70,000 cases of a popular deodorant over unspecified issues potentially related to manufacturing. According to the agency, Pennsylvania-based firm A.P. Deauville ...