A major recall has been issued for more than 67,000 cases of Power Stick roll-on antiperspirant deodorants, after U.S. Food and Drug Administration (FDA) reports cited “cGMP deviations” — meaning the products may have been manufactured outside of FDA’s Current Good Manufacturing Practices. The recall, initiated by A.P. Deauville, affects several variants of the brand’s … Continue reading Over 67,000 Cases of Power Stick Deodorant Recalled Due to FDA Violations