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.

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

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

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

A.P. Deauville recalled over 67,000 cases of Power Stick roll-on deodorants. The recall happened because the products did not follow FDA safety rules. The affected deodorants include Powder Fresh, Spring Fresh,

CHICAGO - A recall is underway for tens of thousands of cases of Power Stick antiperspirant deodorant, according to the FDA; two Chicago women allegedly stole clothes from an Oak Brook store and led police on a high-speed chase; and what started as a playful concert tradition turned into a viral PR nightmare for two tech executives.