#healthsafetyalert
Power Stick antiperspirant recall issued over manufacturing compliance concerns
The Food and Drug Administration (FDA) has announced a nationwide recall affecting over 67,000 cases of Power Stick roll-on antiperspirant deodorants. The enforcement action was initiated by manufacturer A.P. Deauville following concerns about deviations from Current Good Manufacturing Practices (cGMP), which are mandatory quality standards for facilities that produce regulated products like deodorants. According to the official FDA enforcement report, the recall was formally initiated on Jul
Power Stick antiperspirant recall issued over manufacturing compliance concerns
The Food and Drug Administration (FDA) has announced a nationwide recall affecting over 67,000 cases of Power Stick roll-on antiperspirant deodorants. The enforcement action was initiated by manufacturer A.P. Deauville following concerns about deviations from Current Good Manufacturing Practices (cGMP), which are mandatory quality standards for facilities that produce regulated products like deodorants. According to the official FDA enforcement report, the recall was formally initiated on Jul









