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.

Over 60,000 cases of deodorant, which were distributed nationwide, are being recalled.