REGULATORY INTELLIGENCE·Warning Letter
FDA Class II Recall: A.P. Deauville's Antiperspirant Pulled Over CGMP Deviations
A.P. Deauville, LLC has initiated a U.S. nationwide Class II recall for 21,265 cases of its Power Stick for her Roll-On Antiperspirant Deodorant due to Current Good Manufacturing Practice (CGMP) deviations. This action, impacting a key over-the-counter product containing Aluminum Sesquichlorohydrate, signals significant regulatory compliance risks for procurement and regulatory affairs teams. The ongoing recall underscores the critical need for robust quality assurance.
90-Day Activity
A.P. Deauville, LLCExtreme Blast 48h Antiperspirant Deodorant
MKMeera Krishnan· Senior Regulatory Intelligence Analyst2025-07-23