More than 67,000 cases of deodorant have been recalled at the peak of summer. Manufacturer A.P. Deauville and the U.S. Food and Drug Administration (FDA) announced the recall, which affects three varieties of Power Stick deodorant,

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.

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.

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,

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