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

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

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

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.

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.