The fda deodorant recall has become a major talking point in the USA this year as thousands of consumers have searched for answers about deodorant recalled, deodorants recalled, and exactly what it means for their favorite personal care products. With recent headlines highlighting the widespread power stick deodorant recall, it’s never been more important for Americans to stay informed about what’s in their daily hygiene products. This article breaks down everything you need to know about the recall, from why it happened and which deodorants were recalled, to what steps you should take.
Why Was the FDA Deodorant Recall Issued?
In July 2025, the FDA deodorant recall made national news after the Food and Drug Administration (FDA) ordered a voluntary recall of over 67,000 cases of Power Stick products. The affected deodorants, produced by A.P. Deauville in Pennsylvania, were recalled due to “current Good Manufacturing Practice” (cGMP) deviations detected during regulatory checks. cGMP regulations are crucial in guaranteeing that products are safe, effective, and properly made. When any part of the manufacturing process doesn’t meet strict FDA standards, a recall is issued to protect consumer health.
Which Deodorants Were Recalled?
The main products affected by this deodorant recall include several roll-on antiperspirant and deodorant varieties sold across major retailers like Walmart, Dollar Tree, and Amazon. While deodorants recalled can sometimes include many brands, this case was focused on specific Power Stick items made by A.P. Deauville.
Table: List of Power Stick Deodorants Recalled (July 2025)
| Product Name | Type | Scent | Cases Recalled | Lot Numbers (Examples) |
| Power Stick For Her Roll-On Antiperspirant Deodorant (Powder Fresh) | Roll-On Antiperspirant | Powder Fresh | 21,265 | 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402 |
| Power Stick Invisible Protection Roll-On Antiperspirant Deodorant | Roll-On Antiperspirant | Spring Fresh | 22,482 | 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231 |
| Power Stick Original Nourishing Invisible Protection Roll-On | Roll-On Antiperspirant | Original | 23,467 | 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091, 111626G221 |
The recall is significant, affecting Power Stick deodorant products sold nationwide. The products were often found in value packs both in-store and online, so consumers across the United States are advised to check their personal stock carefully.
What Are cGMP Deviations and Why Do They Matter?
When a deodorant recall stems from cGMP deviations, it means there were lapses somewhere in the manufacturing supply chain or process that could impact product safety or quality. Typical cGMP concerns can include improper sanitation, inadequate labeling, process errors, or incomplete quality checks. Although no reported injuries or illnesses were directly linked to these deodorants as of July 2025, the FDA states that cGMP rules exist to ensure that products are exactly as labeled and safe for regular use.
Highlight Points:
- The exact nature of the manufacturing deviation was not disclosed by A.P. Deauville or the FDA.
- Deviations were severe enough for a nationwide recall to be considered necessary as a precaution for consumer safety.
- No other products (like shampoo or body wash) from the manufacturer are affected.
How Can Consumers Identify Recalled Deodorants?
Consumers should look for the specific product names, scents, and lot numbers listed in the table above. These Power Stick deodorants were available at major US retailers and online, including large chains like Walmart and Dollar Tree. Each stick deodorant recalled carries identifiable lot numbers, usually found on the bottom or back of the product packaging.
Quick Steps to Check Your Deodorant:
- Compare the product name, size, and scent with the recall notice.
- Find and match the lot number on your deodorant with those listed in the official recall.
- If your product is part of the deodorant recall, stop use immediately and follow the return or disposal instructions from your retailer or A.P. Deauville.
Marketplace and Health Impacts
Although the deodorant recalled in this notice has not been linked to any serious health outbreaks or injuries, recurring recalls stress the importance of rigorous oversight in the personal care industry. In recent years, deodorants recalled for various safety reasons (including possible benzene contamination or label errors) have raised consumer awareness of the need for transparency and caution.
Consumer Tip: If you have sensitive skin or allergies, always check product recall lists and consider safer, dermatologist-tested alternatives in your daily routine.
What To Do If Your Deodorant Is Recalled
If you discover that your deodorant is among those recalled:
- Do not use the product any further.
- Check your retailer’s recall policy. Many stores will offer a refund or replacement if you return the product with proof of purchase.
- Dispose of the deodorant according to local waste management guidelines or those specified by the recall statement, especially if the product may be hazardous.
- Report any health reactions to the FDA’s MedWatch portal or your healthcare provider.
The FDA deodorant recall is part of a nationwide initiative to prevent future incidents and ensure public trust in personal care products.
Table: Common Deodorant Recall Steps for Consumers
| Step | Action Required |
| Identify recalled product | Check product name, scent, lot # |
| Stop using the product | Dispose or return immediately |
| Request refund or replacement | Contact the retailer |
| Monitor for symptoms/skin reactions | Consult medical professional if needed |
| Stay updated on recalls | Visit FDA website, company news |
Frequently Asked Questions – FDA Deodorant Recall
Q: Why did the FDA recall Power Stick deodorant in 2025?
A: The deodorant recall was announced due to current Good Manufacturing Practice (cGMP) deviations—meaning some part of the production process failed to meet required quality and safety standards.
Q: Is every Power Stick deodorant or other brands affected?
A: No. Only specific lots and scents of Power Stick stick deodorant recall products were affected. The recall does not apply to other deodorant brands or additional Power Stick products like shampoos or body washes.
Q: Where were recalled deodorants sold?
A: Walmart, Dollar Tree, Amazon, and other major retailers nationwide offered these deodorants for sale.
Q: What are cGMP deviations?
A: They are breaches of the FDA’s Current Good Manufacturing Practices, which are rules that guarantee product safety, strength, and quality from raw manufacturing to packaging.
Q: What should I do if I find a recalled deodorant at home?
A: Stop use immediately, return to your retailer if possible, or safely dispose of the product. No adverse incidents have been reported, but it’s always better to follow official guidance.
Q: Will I get sick if I used a recalled deodorant?
A: As of now, there are no reports of health impacts from the recalled lots. However, safety can’t be guaranteed if a product didn’t meet FDA manufacturing standards.
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