A.P. Deauville recalls Power Stick original nourishing invisible protection roll-on antiperspirant/deodorant due to CGMP deviations. Affected lots from 031726A991 to 111626G231. No remedy specified in recall notice.
CGMP Deviations
A.P. Deauville is recalling their Power Stick antiperspirant/deodorant product due to manufacturing quality control issues. This recall does not include a specific action for consumers since the remedy is not stated in the recall notice.
CGMP deviations refer to failures in the manufacturing process that could lead to product quality issues. These deviations might affect the safety and effectiveness of the antiperspirant/deodorant product.
Owners of the Power Stick antiperspirant/deodorant with lot numbers from 031726A991 to 111626G231 are affected. People using this product in normal conditions may be at risk due to the manufacturing deviations.
Check the lot number on the product label, which ranges from 031726A991 to 111626G231. The product is a 1.8 oz./53 mL roll-on antiperspirant/deodorant with NDC# 42913-039-00 and UPC 815195018194.
Look for the lot number on the product label, which should be one of the listed numbers: 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231.
The recall notice does not specify any remedy or action for consumers.
The product is A.P. Deauville Power Stick original nourishing invisible protection roll-on antiperspirant/deodorant. Affected lot numbers range from 031726A991 to 111626G231.
The recall notice states there were CGMP deviations, which could affect product safety, but no specific risk is described in the notice.
We’ve drafted a message you can send A.P. Deauville to request your refund or repair — edit it as you like.
Subject: Recall D-0549-2025 — A.P. Deauville A.P. Deauville Hello, I own a A.P. Deauville that is covered by recall D-0549-2025 from A.P. Deauville. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
