Power Stick for her roll-on antiperspirant recalled over manufacturing deviations
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent is being recalled because of CGMP deviations. 21,265 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
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz (53 mL), from A.P. Deauville, LLC of Pennsylvania, NDC 42913-038-00, UPC 815195019313, is being recalled. The action covers 21,265 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 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381 and 082526E341, 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
- Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-038-00, UPC Code 815195019313
- Manufacturer
- A.P. Deauville, LLC
- Category
- Drug — Antiperspirant
- Affected units
- 21,265
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 (8)
- Lot # 032026B011
- 032226B031
- 051626C241
- 061526C882
- 071226D371
- 071226D381
- 082526E341
- 082826E402
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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