The U.S. Food and Drug Administration (FDA) has issued a voluntary recall of 67,214 cases of Power Stick deodorants, following a July 10 safety notice. The affected products—sold at Walmart, Dollar Tree, Amazon, and other retailers—are being removed due to Current Good Manufacturing Practice (cGMP) violations, which are critical for ensuring consistent quality and consumer safety.
What Triggered the Deodorant Recall?
FDA inspectors discovered that A.P. Deauville, the Pennsylvania-based manufacturer of Power Stick products, failed to comply with cGMP standards, essential for guaranteeing that deodorants contain stated ingredients, potency, and purity. While no health incidents or injuries have been linked to the deodorants, regulators emphasize that manufacturing protocol violations might affect product efficacy or safety.
A.P. Deauville is a personal care product manufacturer based in Easton, Pennsylvania. The company produces a range of personal care items, including deodorants, shampoos, conditioners, and body washes. At this time, no other products from A.P. Deauville have been affected by this recall.
Affected Products
The recall affects the following Power Stick deodorant products:
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Power Stick for Her Roll-On Antiperspirant Deodorant, Powder Fresh (1.8 oz/53 mL): Lot numbers include 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402.
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Power Stick Invisible Protection Roll-On Antiperspirant Deodorant, Spring Fresh (1.8 oz/53 mL): Lot numbers include 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231.
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Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant (1.8 oz/53 mL): Lot numbers include 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091, 111626G221.
These products were distributed nationwide and sold at major retailers, including Walmart, Dollar Tree, and Amazon.
Reason for The Recall
The recall was initiated due to deviations from the FDA’s cGMP regulations. While the specific nature of the manufacturing issues has not been disclosed, cGMP violations can lead to concerns about product safety and quality. Consumers are advised to stop using the affected products and properly dispose of them.
What Consumers Should Do
Consumers who have purchased the recalled Power Stick deodorants should:
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Stop using the affected products immediately.
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Dispose of the products in accordance with local regulations.
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Contact the retailer where the product was purchased for information on returns or refunds.
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Monitor for any adverse reactions and consult a healthcare professional if necessary.
The FDA’s recall of over 67,000 cases of Power Stick deodorants highlights the importance of adhering to manufacturing regulations to ensure product safety and quality. Consumers are urged to check their products against the recalled lot numbers and take appropriate action if they have purchased any of the affected items. For more information, consumers can visit the FDA’s website or contact the retailer where the product was purchased.
