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 difference in the Current Good Manufacturing Practice regulations the FDA oversees.

The FDA has issued a voluntary recall of over 67,000 cases of Power Stick roll-on deodorants due to deviations from manufacturing standards. A.P. Deau

More than 67,000 cases of deodorant sold at major retailers are being recalled due to a manufacturing issue. According to a notice from the FDA, Pennsylvania-based cosmetics brand A.P. Deauville has launched a recall for over 67,000 cases of “Power Fresh” deodorant, including: