Power Stick Antiperspirant Deodorants recalled due to cGMP deviations, United States

United States

A.P. Deauville, LLC has initiated a voluntary recall of its Power Stick roll-on antiperspirant deodorants due to cGMP deviations. The affected products were distributed nationwide in the United States. A total of 67,214 cases are affected.

AFFECTED PRODUCTS:

1) PRODUCT: Power Stick for Her Roll-On Antiperspirant Deodorant Powder Fresh
- 1.8 oz / 53 mL
- UPC Code: 815195019313
- NDC #: 42913-038-00
- Product Quantity: 21,265 cases
- Lot # 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402

2) PRODUCT: Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spring Fresh
- 1.8 oz / 53 mL
- UPC Code: 815195018194
- NDC #: 42913-039-00
- Product Quantity: 22,482 cases
- Lot # 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231

3) PRODUCT: Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant
- 1.8 oz / 53 mL
- UPC Code: 815195018224
- NDC #: 42913-040-00
- Product Quantity: 23,467 cases
- Lot # 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091, 111626G221

The issue was discovered through internal quality checks. The recall was initiated on July 10, 2025, and is currently ongoing. The products have not yet been classified by the FDA.

If you or a loved one is harmed or experiencing any symptoms, it is important to report it. Reporting can help to detect & resolve outbreaks early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.

Source: www.accessdata.fda.gov/scripts/ires/