FDA Deodorant Recall: Over 67,000 Power Stick Units Pulled Nationwide – What You Need to Know

The FDA Deodorant Recall has raised national concerns as more than 67,000 units of popular Power Stick deodorants are being pulled from store shelves and online platforms. The recall, classified as Class II by the U.S. Food and Drug Administration (FDA), signals possible temporary or medically reversible health risks.

This significant FDA Deodorant safety alert was initiated by A.P. Deauville, a Pennsylvania-based manufacturer, on July 10, 2025, and later classified by the FDA on July 31, 2025. The recalled products were sold nationwide through major retailers like Dollar Tree, Amazon, Walmart, and more.

Why the FDA Deodorant Recall Matters

The FDA Deodorant recall is linked to violations of Current Good Manufacturing Practice (CGMP) regulations. These are strict guidelines that ensure personal care products meet standards for identity, strength, quality, and purity.

While the FDA has not provided full details on the violations, the Class II designation means the product may cause short-term, reversible health issues such as skin irritation or mild allergic reactions, though serious consequences are unlikely.

This is not the first time A.P. Deauville has faced regulatory issues. In 2005, the company reached a $50,000 settlement with the California Air Resources Board for allegedly exceeding volatile organic compound limits in their deodorants.

Products Affected by the FDA Deodorant Recall

Three Power Stick roll-on antiperspirants are part of the Deodorant recall:

1. Power Stick for Her Roll-On Antiperspirant Deodorant (Powder Fresh)
   • Size: 1.8 oz / 53 mL
   • UPC: 815195019313
   • NDC: 42913-038-00
   • Lot Codes: 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402
   • Quantity: 21,265 cases
2. Power Stick Invisible Protection Roll-On Antiperspirant Deodorant (Spring Fresh)
   • Size: 1.8 oz / 53 mL
   • UPC: 815195018194
   • NDC: 42913-039-00
   • Lot Codes: 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231
   • Quantity: 22,482 cases
3. Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant (Original)
   • Size: 1.8 oz / 53 mL
   • UPC: 815195018224
   • NDC: 42913-040-00
   • Lot Codes: 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091, 111626G221
   • Quantity: 23,467 cases

How to Check if Your Product Is Part of the FDA Deodorant Recall

If you have purchased any FDA Deodorant-related products recently, check the UPC code and lot number printed on your deodorant container. If they match the recalled batches, stop using the product immediately.

The FDA recommends returning recalled deodorants to the retailer for a refund or following safe disposal instructions from the manufacturer.

The Manufacturer’s Statement

A.P. Deauville addressed the FDA Deodorant recall on its website:

“Our antiperspirant/deo sticks and shower products are manufactured in our FDA-regulated factory. We choose to own our factory and make our product rather than outsourcing, to ensure the best quality and affordability for our customers.”

Possible Health Concerns

While the FDA Deodorant recall is preventive, it’s important to remain cautious. A Class II recall means skin irritation, allergic reactions, or other short-term effects are possible. If you notice any symptoms after using a recalled deodorant, stop use immediately and consult a healthcare provider.

Industry Context: Safety and Sustainability

The FDA Deodorant recall is part of a broader conversation about personal care product safety. In recent years, recalls have targeted deodorants containing harmful chemicals like benzene.

At the same time, the industry is evolving — for example, Wild, a refillable deodorant brand, was recently acquired by Unilever for £100 million, proving that safe and sustainable deodorants are in demand.

What to Do If You Have a Recalled FDA Deodorant Product

1. Check UPC codes and lot numbers.
2. Stop using recalled products immediately.
3. Follow return or disposal instructions from the retailer or manufacturer.
4. Report any adverse effects to the FDA’s MedWatch system.

Stay informed and protect your health. For more important consumer safety alerts, visit our Health News Section.