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 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.

More than 67,000 cases of Power Stick deodorants are being recalled due to safety concerns tied to manufacturing practices, the FDA warns.

As temperatures soar in Texas, a recall of over 67,000 cases of deodorants prompts shoppers to verify their products from retailers.

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.