The FDA Deodorant Recall is making headlines as more than 67,000 units of Power Stick deodorants have been urgently pulled from shelves across the United States after regulatory inspections revealed violations of Current Good Manufacturing Practices (cGMP). This sweeping recall, announced by the FDA and executed by Pennsylvania-based manufacturer A.P. Deauville on July 10, 2025, has sent shockwaves through consumers who depend on these products for daily hygiene.
Major retailers such as Walmart, Amazon, and Dollar Tree have removed these deodorants from inventory. Consumers who purchased any affected items should review their products immediately and follow FDA recommendations.
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Which Power Stick Products Are Affected?
Three specific roll-on antiperspirant deodorants are included in the recall. All are packaged in 1.8-ounce containers:
- Power Stick for Her Roll-On Antiperspirant Deodorant – Powder Fresh (21,265 cases)
- Power Stick Invisible Protection Roll-On Antiperspirant Deodorant – Spring Fresh (22,482 cases)
- Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant (23,467 cases)
These products were distributed nationwide and sold both in-store and online.
| Product Name | Package Size | Cases Recalled |
|---|---|---|
| Power Stick for Her Powder Fresh | 1.8oz | 21,265 |
| Power Stick Spring Fresh | 1.8oz | 22,482 |
| Power Stick Original Nourishing | 1.8oz | 23,467 |
Why Did the FDA Recall Power Stick Deodorants?
Regulatory inspections found that A.P. Deauville did not meet FDA cGMP standards. This means there may have been contamination, improper ingredient measurements, or oversight in labeling or packaging during production. While there haven’t been any injuries or adverse health reports so far, the FDA noted these manufacturing issues could pose safety risks, especially for those with sensitive skin or underlying conditions.
Key issues behind the recall include:
- Contamination risks during production.
- Inaccurate ingredient measurements.
- Labeling or packaging mistakes.
- Failed sterile environment controls.
What Should Consumers Do?
If you possess any of the recalled Power Stick deodorants, the FDA provides clear guidance:
- Stop using the product immediately.
- Dispose of the deodorant or return it to the retailer for a refund.
- Contact A.P. Deauville directly for instructions if necessary.
There have been no reported side effects or injuries at this time, but out of an abundance of caution, discontinuing use is strongly advised.
How to Identify Recalled Lot Numbers
Affected deodorants have specific lot numbers printed on the packaging. The FDA’s website lists all impacted lot codes. Double-check your product label against the following lot numbers:
Powder Fresh: 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402
Spring Fresh: 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231
Original Nourishing: 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091, 111626G221.
What’s Next?
This massive FDA deodorant recall sends a powerful message to manufacturers and consumers alike about the importance of strict quality control and safety standards. If you purchased a Power Stick deodorant recently, check your product against the information above and take the recommended steps promptly.
Have you been affected by the FDA Deodorant Recall? Share your experience or concerns in the comments below—your insights can help others stay safe and informed.