TL;DR

• Power Stick deodorants recalled at Walmart, Dollar Tree, and Amazon.
• 67,000+ cases affected due to manufacturing violations (cGMP deviations).
• Check lot numbers—if yours matches, stop using and return it.
• No reported injuries, but FDA advises caution.

FDA issues recall for over 67,000 cases due to manufacturing violations—here’s how to check if your deodorant is affected

Thousands of Power Stick antiperspirant deodorants sold at major retailers, including Walmart, Dollar Tree, and Amazon, have been recalled due to manufacturing violations, according to a U.S. Food and Drug Administration (FDA) enforcement report. The recall, initiated by manufacturer A.P. Deauville on July 10, affects multiple scents and lot numbers, raising concerns about product safety.

Here’s what consumers need to know—including how to identify recalled products, why they were pulled, and what to do if you own one.

Which Power Stick Deodorants Are Recalled?

The recall includes three types of Power Stick roll-on antiperspirants, totaling more than 67,000 cases distributed nationwide. The affected products are:

1. Power Stick for Her Roll-On Antiperspirant Deodorant (“Power Fresh” scent)
2. Power Stick Invisible Protection Roll-On Antiperspirant Deodorant (“Spring Fresh” scent)
3. Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant

How to Check Your Deodorant’s Lot Number

The recall applies to specific lot numbers printed on the packaging. If you own any of the following, discontinue use immediately:

Power Stick for Her (“Power Fresh”) Recalled Lots:

• 032026B011
• 032226B031
• 051626C241
• 061526C882
• 071226D371
• 071226D381
• 082526E341
• 082826E402

Power Stick Invisible Protection (“Spring Fresh”) Recalled Lots:

• 031726A991
• 041226B561
• 062026C901
• 062026C911
• 071026D351
• 071026D361
• 071326D391
• 111626G231

Power Stick Original Nourishing Recalled Lots:

• 101225D781
• 032926B281
• 032826B221
• 041126B531
• 062226D011
• 070626D301
• 070626D333
• 111026G051
• 111326G091
• 111626G221

Why Were These Power Stick Deodorants Recalled?

The FDA classified this as a Class II recall, meaning the affected products may cause temporary or medically reversible adverse health consequences. The recall was triggered by “cGMP deviations”—violations of the Current Good Manufacturing Practice (cGMP) regulations, which ensure product quality and safety.

What Are cGMP Violations?

• cGMP standards require proper controls in production, testing, and storage.
• Deviations could mean contamination, incorrect labeling, or improper ingredient measurements.
• While no injuries have been reported, the FDA advises discontinuing use as a precaution.

Where Were These Products Sold?

The recalled deodorants were distributed nationwide and sold at:

• Walmart
• Dollar Tree
• Amazon
• Other regional retailers

A.P. Deauville, the manufacturer, operates an FDA-regulated facility in Pennsylvania and also produces shampoos, conditioners, and body washes.

What Should Consumers Do?

If you own a recalled Power Stick deodorant:

1. Stop using it immediately.
2. Check the lot number against the FDA’s list.
3. Return it to the place of purchase for a refund or exchange.
4. Contact A.P. Deauville (if needed) at [company contact info].

Has There Been a Similar Recall Before?

This isn’t the first time a deodorant recall has made headlines:

• 2023: Procter & Gamble recalled Old Spice and Secret aerosol sprays due to benzene contamination.
• 2021: Unilever pulled Dove, Nexxus, and TRESemmé dry shampoos over carcinogen concerns.

Final Thoughts: Should You Be Worried?

While no injuries have been reported, the FDA’s recall is a precautionary measure due to potential manufacturing issues. Consumers should:
Check their deodorant lot numbers.
Follow FDA guidelines for returns.
Stay updated on further announcements.

For now, switching to an alternative antiperspirant brand may be the safest choice.

TL;DR

• Power Stick deodorants recalled at Walmart, Dollar Tree, and Amazon.
• 67,000+ cases affected due to manufacturing violations (cGMP deviations).
• Check lot numbers—if yours matches, stop using and return it.
• No reported injuries, but FDA advises caution.

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