More than 67,000 cases of Power Stick deodorant have been recalled because they failed to meet safety and quality standards, according to the U.S. Food and Drug Administration.

According to the FDA, 67,000 cases of Power Stick deodorant have been recalled. The recall was initiated on July 10, and it applies to the following products from the brand: Power Stick for Her Roll-On Antiperspirant Deodorant Powder Fresh, 1.8 oz/ 53 mL UPC Code 815195019313

More than 67,000 cases of roll-on deodorant that were sold nationwide have been voluntarily recalled due to an undisclosed manufacturing defect.

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

Over 67,000 cases of “Power Stick” roll‑on deodorant recalled by A.P. Deauville due to cGMP violations. Three variants are included – Power Stick F

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

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

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

The FDA is sounding the alarm with a deodorant recall that is impacting more than 67,000 cases of antiperspirant made by a popular manufacturer.