Last week, the United States Food and Drug Administration (FDA) and A.P. Deauville issued a voluntary recall for over 67,000 cases of Power Stick deodorant due to “cGMP deviations,” which is a difference in the Current Good Manufacturing Practice regulations the FDA oversees.

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 deodorant have been recalled nationwide due to safety concerns.The recall affects three Powder Stick deodorant products, made by A.P. Deuville, LLC.Check if your deodorant is part of the recall,