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

The Food and Drug Administration has recalled more than 67,000 cases of deodorant sold at major retailers due to ...

A.P. Deauville, a Pennsylvania-based health and beauty manufacturer, has recalled more than 67,000 cases of its Power Stick roll-on deodorants.

CHICAGO - A recall is underway for tens of thousands of cases of Power Stick antiperspirant deodorant, according to the FDA; ...

The FDA and Power Stick recalled thousands of deodorant cases because manufacturing practices did not comply with FDA standards. Here are the affected products.

More than 67,000 cases of Power Stick antiperspirant deodorant sold nationwide have been voluntarily recalled due to ...

The FDA did not provide a reason for the recall, but said the products had a cGMP (Current Good Manufacturing Practices) deviation.

Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.

On July 10, Pennsylvania-based health and beauty manufacturer A.P. Deauville announced a recall of 67,214 cases of its Power ...

More than 67,000 cases of Power Stick deodorant were recalled nationwide after a manufacturing issue raised concerns about product quality.

Last week, the United States Food and Drug Administration (FDA) and A.P. Deauville issued a voluntary recall for over 67,000 cases of Power Stick deodorant due to “cGMP deviations,” which is a ...

Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by the FDA.