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.

But one thing we’re confident about is that nobody wants to use a deodorant that has been recalled, which is why we are sharing this news: The Food and Drug Administration has issued a recall on 67,000 cases of Power Stick antiperspirant deodorant.

On July 10, Pennsylvania-based health and beauty manufacturer A.P. Deauville announced a recall of 67,214 cases of its Power Stick roll-on deodorant due to violations of Current Good Manufacturing Practice (CGMP) standards, a set of FDA-enforced guidelines designed to ensure product safety and quality.

Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.

More than 67,000 cases of Power Stick roll-on deodorant products have been recalled. They were sold at Target, Walmart, Amazon and more.

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.

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