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    Home»Business»67,000 cases of deodorant recalled for undisclosed manufacturing issue
    Business

    67,000 cases of deodorant recalled for undisclosed manufacturing issue

    Justin M. LarsonBy Justin M. LarsonJuly 16, 2025No Comments2 Mins Read
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    FDA Commissioner Marty Makary on ensuring prescription drug prices decrease, restoring trust in public health and integrating artificial intelligence into the federal agency.

    A recall is underway for tens of thousands of cases of Power Stick antiperspirant deodorant, according to the Food and Drug Administration (FDA).

    An enforcement report published by the agency showed A.P. Deauville launched a recall for over 67,000 cases of “power fresh”-scented Power Stick for Her Roll-On Antiperspirant Deodorant, “spring fresh”-scented Power Stick Invisible Protection Roll-On Antiperspirant Deodorant and Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant. 

    FDA HQ sign in Maryland

    A sign outside Food and Drug Administration headquarters July 20, 2020, in White Oak, Md. (Sarah Silbiger/Getty Images / Getty Images)

    The company took that step July 10, according to the report.

    BREAD SOLD AT WALMART, KROGER RECALLED DUE TO UNDECLARED POTENTIALLY LIFE-THREATENING ALLERGEN

    The lot numbers of the recalled cases of Power Stick for Her Roll-On Antiperspirant Deodorant were 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341 and 082826E402, while the lot numbers for the affected Power Stick Invisible Protection Roll-On Antiperspirant included 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391 and 111626G231, the FDA enforcement report said.

    For the third variety, the lot numbers 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091 and 111626G221 were among those recalled.

    ABOUT 49K ELECTRIC CHAINSAWS, POLE SAWS RECALLED FOR SWITCH FAILURE LACERATION HAZARD

    The enforcement report identified “cGMP deviations” as what prompted the recall, indicating it was related to the Current Good Manufacturing Practice regulations the FDA oversees. 

    FDA headquarter sign

    FDA headquarters in Washington, D.C. (iStock / iStock)

    A.P. Deauville says on its website it makes its antiperspirant deodorants at its “FDA-regulated” factory in Pennsylvania. 

    The cases of the recalled Power Stick deodorant were shipped nationwide, according to the FDA enforcement report. The deodorant is sold at Walmart, Dollar Tree and Amazon. 

    YOCRUNCH YOGURTS RECALLED FOR POSSIBLE PLASTIC PIECES IN TOPPERS

    A.P. Deauville is based in Easton, a city in eastern Pennsylvania that sits near the state’s border with neighboring New Jersey.

    In addition to deodorant, the company makes shampoos, conditioners, lotion, body washes and facial wipes, according to its website. 



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