The FDA remembers more than 67,000 cases of deodorants

For safety reasons, more than 67,000 cases of deodorant were recalled nationwide.

On Thursday, July 10th, the US Food and Drug Administration announced a nationwide recall of some Power -Stick -Deodorants manufactured by AP Deauville.

The recall was voluntary and comprises 21,265 cases of power for your roll-on antitranspirant deodorant powder; 22,482 Cases of Kraftstab Invisible protection adaptation deodorant fresh statement; and 23,467 Power Stick Original Nourishing Invisible Protection Roll-On-Antiperant Deodorant.

The FDA states that the recall is due to “CGMP deviations”. The agency's website finds that CGMP stands for “current good manufacturing practice” and that these regulations “ensure that a product is secure and that it has the ingredients and the strength it claims.”

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The products were shipped nationwide and sold to large retailers such as Walmart, Dollar Tree and Amazon.

AP Deauville did not immediately respond to people's request for comments. However, the FDA usually encourages consumers who bought back products to stop the use and dispose of the items.

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