Massive Recall Alert: 67,000 Cases of Power Stick Deodorant Pulled Over Manufacturing Concerns

By News Updates 24 Staff

Published: July 24, 2025

In a significant consumer alert, the U.S. Food and Drug Administration (FDA) has issued a recall for approximately 67,000 cases of Power Stick roll-on deodorants, due to deviations from Current Good Manufacturing Practices (CGMP) — a set of federal guidelines that ensure the safety and quality of consumer products.

The recall was officially announced on July 10, 2025, and includes three popular variants of Power Stick antiperspirant deodorant:

Products Under Recall:

• Power Stick for Her Roll-On Antiperspirant Deodorant – Powder Fresh
  Size: 1.8 oz / 53 mL
  UPC Code: 815195019313

• Power Stick Invisible Protection Roll-On Antiperspirant Deodorant – Spring Fresh
  Size: 1.8 oz / 53 mL
  UPC Code: 815195018194

• Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant
  Size: 1.8 oz / 53 mL
  UPC Code: 815195018224

What the FDA Says

The FDA has not disclosed a specific health risk associated with the products but cited non-compliance with federal manufacturing standards. While no injuries or adverse effects have been reported so far, the agency emphasizes that CGMP violations can potentially lead to compromised product safety or performance.

“Consumers deserve to know that the personal care items they use daily are manufactured under the highest quality standards,” an FDA spokesperson said in a public notice.

Where These Products Were Sold

The recalled deodorants were distributed nationwide and are commonly found at Dollar Tree, Walmart, and Amazon, among other retailers. Due to the wide distribution, the FDA recommends that consumers check their products carefully using the UPC codes listed above.

What Should Consumers Do?

While the manufacturer has not yet provided a clear return or refund process, the general recommendation for consumers is to stop using any of the recalled products immediately. Holding onto the packaging and receipts may help with any future return or exchange instructions.

If you believe you’ve been affected or have experienced adverse reactions, it’s advised to contact your healthcare provider and report the issue to the FDA’s MedWatch program.

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For further developments and official guidance, visit the FDA's Recalls & Safety Alerts page or follow News Updates 24 for real-time updates on product recalls and consumer safety news.

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