Various Power Stick deodorants have been recalled due to "Current Good Manufacturing Practice deviations", according to the U ...

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

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 ...

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 ...

New York-based Krasniy Oktyabr Inc. USA is recalling a fish product due to the potential risk of botulism poisoning.

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

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 ...

A popular line of roll-on deodorants is being recalled after safety issues were discovered during manufacturing.A.P.

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

More than 67,000 cases of Power Stick deodorants were recalled for deviating from Food and Drug Administration standards.