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.

The FDA has announced a recall of 70,000 cases of Power Stick deodorant due to safety and quality concerns. These products were sold on Amazon, Dollar Tree, and Walmart.The recall affects three types of deodorant that did not meet manufacturing regulations,