Power Stick roll-on antiperspirant recalled over manufacturing practice deviations
Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant is being recalled because of CGMP deviations. 23,467 cases are affected.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II recall for manufacturing practice deviations with no contamination, potency failure or health consequence stated in the source.
Plain-English summary
Shave and Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant, 1.8 oz (53 mL), from A.P. Deauville, LLC of Pennsylvania, NDC 42913-040-00, UPC 815195018224, is being recalled. The action covers 23,467 cases.
The stated reason is CGMP deviations, meaning departures from current good manufacturing practice. The FDA classified the action as Class II. The source does not describe a resulting health consequence.
Affected lots include 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301 and 070626D333, together with the further lots listed in the recall notice. Distribution was nationwide in the United States.
Consumers who have an affected lot should stop using it and follow the instructions issued by the firm.
The recalled product
- Product
- Shave and Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant, 1.8 oz./ 53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-040-00 UPC Code 815195018224
- Manufacturer
- A.P. Deauville, LLC
- Category
- Drug — Antiperspirant
- Affected units
- 23,467
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (10)
- Lot # 101225D781
- 032926B281
- 032826B221
- 041126B531
- 062226D011
- 070626D301
- 070626D333
- 111026G051
- 111326G091
- 111626G221
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by A.P. Deauville, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
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