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.

More than 67,000 cases of Power Stick deodorants were recalled for deviating from Food and Drug Administration standards.

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