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Power Stick roll-on deodorants are being pulled from shelves due to safety concerns flagged by the FDA. More than 67,000 cases are affected in the nationwide recall.

Power Stick Deodorant Recall: 67,000+ Cases Recalled by FDA

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  • Post last modified:July 21, 2025

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Power Stick Deodorant Recall: FDA Pulls 67,000+ Cases Nationwide

Introducing a major nationwide alert: Power Stick deodorant recall — over 67,000 cases sold at Walmart, Amazon, and Dollar Tree have been voluntarily pulled by the FDA. This post goes deeper than the rest, offering full clarity on recall details, consumer tips, and what this means for public safety.

What’s Happening? The Recall Unpacked

On July 10, 2025, the U.S. Food and Drug Administration announced a full-scale recall of Power Stick deodorants made by A.P. Deauville LLC due to violations of the FDA’s Current Good Manufacturing Practices (cGMP). The affected inventory includes:

  • 21,265 cases of Power Stick for Her Roll‑On Antiperspirant (Powder Fresh)
  • 22,482 cases of Power Stick Invisible Protection Spring Fresh
  • 23,467 cases of Power Stick Original Nourishing Invisible Protection

These products were distributed nationwide through Walmart, Amazon, and Dollar Tree, with customers urged to stop using them and dispose of any affected items. People.com

What Are cGMP Violations and Why Do They Matter

The FDA enforces cGMP standards to ensure personal care products are consistently manufactured with proper ingredient strength, purity, and quality controls. Deviations from these practices may:

  • Compromise product safety
  • Lead to labeling or composition errors
  • Increase the risk of contamination

In this case, no illnesses or adverse health incidents have been reported—yet the FDA views cGMP deviations as serious enough to justify a large-scale recall. The Economic Times

Which Lot Numbers Are Affected?

The recall targets specific lot numbers—here are a few examples compiled from multiple FDA enforcement sources:

  • Power Stick for Her: 032026B011, 032226B031, 082526E341, among others
  • Invisible Protection: 031726A991, 041226B561, 071326D391, etc.
  • Original Nourishing: 101225D781, 032926B281, 070626D301, etc.

Consumers should compare their products’ lot codes (found beneath barcodes) against the FDA’s published list before deciding on disposal or return.

Where It Was Sold & Price Insight

These deodorants were sold across major U.S. retailers:
🔹 Walmart – 3‑pack for ~$21
🔹 Dollar Tree – 24‑pack for ~$30
🔹 Amazon – sold individually or in bundles

Despite generally positive reviews (averaging 4.2 ★), the recall reflects quality control concerns, not consumer dissatisfaction. The Sun

Company History & Regulatory Context

A.P. Deauville, based in Pennsylvania, has a portfolio extending beyond deodorant to lotions, shampoos, and facial wipes. Previously in 2005, they settled for $50,000 over excess volatile organic compounds, demonstrating past regulatory scrutiny.

This recall is part of the FDA’s broader push in 2025 to tighten oversight on personal care products. It follows earlier high-profile recalls involving benzene contamination in well‑known skincare lines.

What Should Consumers Do?

  1. Check your product for lot codes underneath the barcode.
  2. Stop using the product immediately if your product matches the recall.
  3. Dispose of it safely or follow the manufacturer’s guidelines for a refund.
  4. Contact A.P. Deauville or the point of purchase for further instructions.

Transparent prompts by major retailers should assist with refunds or replacements.

Why This Recall Matters to You

Even without reported injuries, this event underscores how critical manufacturing standards are in everyday consumer goods. It’s also a case study in how such recalls can:

  • Erode trust, even when a product is symptom-free
  • Show the power of supply chain vigilance
  • Confirm the FDA’s increasing scrutiny of the hygiene and personal care sector

Consumers should stay alert to potential quality-related recalls of widely used goods.

Healthy Habits: Choosing Safer Alternatives

While navigating this recall, consider these steps for safe purchasing:

  • Select brands with transparent manufacturing certifications
  • Avoid bulk buys of personal care products without verifying quality controls
  • Look for clean labels free of questionable additives

Additionally, monitor FDA and retailer websites for any updates on product safety and compliance.

Conclusion

The Power Stick deodorant recall—spanning 67,214 cases—sheds light on how manufacturing lapses can quickly become nationwide alerts. Although no health incidents have been reported to date, this episode underscores the ongoing importance of regulatory oversight and consumer diligence.

Stay informed, verify your products, and exercise caution to protect your health and reputation.

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