Deodorant sold at retailers nationwide has been recalled, according to the U.S. Food and Drug Administration.

Why Power Stick Deodorants Were Recalled

More than 67,000 cases of women's deodorant sold at popular retailers like Walmart, Dollar Tree, and Amazon have been recalled. According to a report shared by the FDA, the recall was initiated due to "cGMP deviations." This suggests that there may have been violations by the manufacturer of the Current Good Manufacturing Practice regulations outlined by the FDA.

The Manufacturer Behind Power Stick Products

The affected deodorants are manufactured by A.P. Deauville, LLC, located in Easton, Pennsylvania, and are sold under the "Power Stick" brand, a household name for consumers for more than 40 years. According to its website, the company purchased the Power Stick brand two decades ago. The company also manufactures shampoos, conditioners, lotions, body washes, and face wipes.

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We take pride in manufacturing and offering products that are great quality at an affordable price. We obsess over every part of products from the color of the barrels to making sure the fragrances are on trend and last long. Our antiperspirant/deo sticks and shower products are manufactured in our FDA regulated factory. We could save money “outsourcing” or not caring enough to make it ourselves, but we CHOOSE to own our factory and make our product. -APDeauville

READ MORE: Eggs Linked to Salmonella Outbreak Linked to Illnesses and Death

Previous FDA Violations Raise Concerns

While the company brags about its devotion to quality, this is not the first time the company has failed to meet the FDA's Current Good Manufacturing Practice regulations. In 2019, A.P. Deauville received a Warning Letter from the FDA for numerous "significant violations," including ignoring important warning signs about water quality and using potentially unsafe water to make a product people use on their bodies.

You received multiple complaints regarding possible allergic reactions to your OTC topical drug products. Some complaints described rashes and blistering; one described an abscess requiring medical attention. You failed to adequately investigate and resolve these customer complaints. - 2019 FDA Warning Letter

Additionally, among the many violations noted by the FDA, the company failed to investigate and resolve customer complaints, and it did not take the necessary steps to ensure processes and equipment consistently made high-quality, reliable products. The full Warning Letter can be found on the FDA website.

What Power Stick Products Are Included in the Recall

Now, in 2025, A.P. Deauville is again facing issues tied to "cGMP deviations" resulting in the recall of 67,000 cases of Power Stick brand deodorants, including the following products, according to the most recent FDA report:

Power Stick for her roll-on Antiperspirant Deodorant Powder Fresh -  1.8 oz/53 mL UPC Code 815195019313
Lot # 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402

Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spring Fresh -1.8 oz/53 mL UPC Code 815195018194
Lot # 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231

Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant - 1.8 oz/ 53 mL UPC Code 815195018224
Lot # 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091, 111626G221

What Consumers Should Do Next

Consumers who may have these products in their homes should stay alert for any additional guidance or direction regarding the recall, and in the meantime, they should not use the products.

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Gallery Credit: Melissa

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