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.

According to the FDA, 67,000 cases of Power Stick deodorant have been recalled. The recall was initiated on July 10, and it applies to the following products from the brand: Power Stick for Her Roll-On Antiperspirant Deodorant Powder Fresh, 1.8 oz/ 53 mL UPC Code 815195019313

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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