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.

Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by the FDA.

More than 67,200 Power Stick deodorants have been recalled due to manufacturing violations, according to the U.S. Food and Drug Administration (FDA).