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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Personal Care & Cosmetics/Skincare

Power Stick Antiperspirant Deodorants Recalled for Manufacturing Deviations

Agency Publication Date: July 14, 2025
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Summary

A.P. Deauville, LLC is recalling approximately 67,214 units of Power Stick brand roll-on antiperspirant deodorants, including the Power Stick for Her, Spring Fresh, and Original Nourishing varieties. This recall was initiated due to deviations from Current Good Manufacturing Practice (CGMP) requirements, which are the federal standards that ensure products are manufactured under safe and high-quality conditions. The products are sold in 1.8 oz (53 mL) bottles and were distributed nationwide across the United States.

Risk

Manufacturing deviations mean the products were not produced according to strict quality control standards, which can potentially lead to safety or effectiveness issues. No specific injuries or adverse health effects have been reported to date.

What You Should Do

  1. This recall affects Power Stick brand roll-on antiperspirant deodorants in 1.8 oz (53 mL) bottles, specifically the 'Power Stick for Her' (Powder Fresh), 'Power Stick Spring Fresh', and 'Power Stick Original Nourishing Invisible Protection' varieties.
  2. Identify your product by checking the NDC numbers (42913-038-00, 42913-039-00, 42913-040-00), the UPC barcodes, and the lot numbers printed on the packaging. See the Affected Products section below for the full list of affected codes.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact A.P. Deauville, LLC for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent (1.8 oz./53 mL)
Variants: Powder Fresh Scent, Roll-On
UPC Codes:
815195019313
Lot Numbers:
032026B011
032226B031
051626C241
061526C882
071226D371
071226D381
082526E341
082826E402
NDC:
42913-038-00

Recall #: D-0548-2025; Quantity: 21,265 cases

Product: Beauty & Skincare Power Stick original nourishing invisible protection roll-on Antiperspirant/Deodorant Spring Fresh (1.8 oz./53 mL)
Variants: Spring Fresh Scent, Roll-On
UPC Codes:
815195018194
Lot Numbers:
031726A991
041226B561
062026C901
062026C911
071026D351
071026D361
071326D391
111626G231
NDC:
42913-039-00

Recall #: D-0549-2025; Quantity: 22,482 Cases

Product: Shave and Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant (1.8 oz./ 53 mL)
Variants: Original Nourishing, Roll-On
UPC Codes:
815195018224
Lot Numbers:
101225D781
032926B281
032826B221
041126B531
062226D011
070626D301
070626D333
111026G051
111326G091
111626G221
NDC:
42913-040-00

Recall #: D-0550-2025; Quantity: 23,467 Cases

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97211
Status: Active
Manufacturer: A.P. Deauville, LLC
Manufactured In: United States
Units Affected: 3 products (21,265 cases; 22,482 Cases; 23,467 Cases)
Distributed To: Nationwide
Agency Last Updated: July 31, 2025

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.