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Power Stick Deodorants Recalled for Manufacturing Issues

Quality issues may pose potential safety risks to consumers


A photo shows a woman applying roll-on antiperspirant in front of white background
Getty Images

This article was created with the assistance of generative AI. It was reviewed by editors before publication.

Over 67,000 cases of Power Stick brand deodorants were recalled because the manufacturing processes didn’t follow standard safety and quality guidelines, according to an enforcement report by the Food and Drug Administration.

The recall involves three Power Stick roll-on antiperspirant deodorant products that were distributed nationwide. Media reports indicate the products were sold at Dollar General, Walmart and Amazon.

The recalled deodorants

The recall includes the following products manufactured by A.P. Deauville:

Power Stick for Her Roll-On Antiperspirant Deodorant Powder Fresh

  • Size: 1.8 ounces/53 milliliters
  • UPC Code: 815195019313
  • NDC#: 42913-038-00
  • Lot Numbers: 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402

Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spring Fresh

  • Size: 1.8 oz/53 mL
  • UPC Code: 815195018194
  • NDC#: 42913-039-00
  • Lot Numbers: 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231

Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant

  • Size: 1.8 oz/53 mL
  • UPC Code: 815195018224
  • NDC#: 42913-040-00
  • Lot Numbers: 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091, 111626G221

Consumers should verify their purchases against the lot numbers and UPC codes provided by the FDA. If a product is identified as part of the recall, it should be returned to the retailer and its use should be discontinued.

The recall is being conducted to ensure consumer safety, as the enforcement report cites “CGMP deviations” which refer to Current Good Manufacturing Practices enforced by the FDA. No adverse effects related to the recalled products have been reported.

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