FDA Proactively Recalls 67,000+ Cases of Power Stick Deodorant to Protect Consumer Safety

The FDA has announced a major recall of more than 67,000 Power Stick deodorants due to manufacturing issues. Learn which products are affected, where they were sold, and how to get a refund.

FDA Proactively Recalls 67,000+ Cases of Power Stick Deodorant to Protect Consumer Safety

A Serious Warning for Deodorant Users Across the U.S.

If you’ve recently purchased a roll-on Power Stick deodorant, it might be time to double-check your bathroom shelf. The U.S. Food and Drug Administration (FDA) has confirmed a sweeping recall of over 67,000 cases of Power Stick antiperspirant deodorants due to manufacturing violations. The products, widely available at popular retailers like Walmart, Dollar Tree, and Amazon, were produced by personal care company A.P. Deauville.

The company voluntarily reported the issue to the FDA and launched the recall following the discovery of deviations from current Good Manufacturing Practices (cGMP). Here’s a detailed breakdown of what happened, which products are affected, and what consumers need to do next.

Why Were Power Stick Deodorants Recalled?

According to the FDA enforcement report published in July 2025, the recall stems from “cGMP deviations” during the manufacturing process. These deviations suggest that certain steps during production did not meet the strict safety and quality standards set by the FDA’s Current Good Manufacturing Practices regulations.

While the report does not cite any specific contamination or health risks, cGMP violations can lead to inconsistencies in product quality or safety—enough to justify a precautionary recall. A.P. Deauville, the company behind the Power Stick brand, initiated the recall voluntarily on July 10, 2025.

Products Included in the Recall

The recall includes three popular varieties of Power Stick roll-on antiperspirant deodorants, all in the standard 1.8 oz (53 mL) size. In total, 67,214 cases have been affected.

FDA Proactively Recalls 67,000+ Cases of Power Stick Deodorant to Protect Consumer Safety

🔹 Power Stick for Her Roll-On Antiperspirant Deodorant – Powder Fresh

  • Quantity recalled: 21,265 cases
  • Fragrance: Powder Fresh
  • Targeted demographic: Women

🔹 Power Stick Invisible Protection Roll-On Antiperspirant Deodorant – Spring Fresh

  • Quantity recalled: 22,482 cases
  • Fragrance: Spring Fresh
  • Type: Invisible protection for daily use

🔹 Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant

  • Quantity recalled: 23,467 cases
  • Type: Original Nourishing formula
  • Design: Long-lasting invisible protection

These roll-ons are a staple in many American households and known for their affordability and availability in discount stores and online retailers.

Affected Lot Numbers: Check Your Product

Consumers are encouraged to check the lot numbers printed on their product packaging. If your deodorant matches any of the lot codes listed below, it falls under the recall.

Power Stick for Her – Powder Fresh

  • 032026B011
  • 032226B031
  • 051626C241
  • 061526C882
  • 071226D371
  • 071226D381
  • 082526E341
  • 082826E402

Power Stick Invisible Protection – Spring Fresh

  • 031726A991
  • 041226B561
  • 062026C901
  • 062026C911
  • 071026D351
  • 071026D361
  • 071326D391
  • 111626G231

Power Stick Original Nourishing – Invisible Protection

  • 101225D781
  • 032926B281
  • 032826B221
  • 041126B531
  • 062226D011
  • 070626D301
  • 070626D333
  • 111026G051
  • 111326G091
  • 111626G221

If you find any of these numbers on your product, it is advised that you stop using it immediately and proceed with the return or refund process.

Where Were These Products Sold?

These deodorants were shipped and sold nationwide across the United States, primarily through:

  • Walmart
  • Dollar Tree
  • Amazon

Due to their affordability, Power Stick products are especially common in discount and bulk-purchase settings, which means the recall could affect a large number of consumers.

FDA Proactively Recalls 67,000+ Cases of Power Stick Deodorant to Protect Consumer Safety

Who Is Behind the Recall? About A.P. Deauville

A.P. Deauville, the manufacturer of Power Stick, is based in Easton, Pennsylvania, and is a long-standing producer of personal care products. Their range includes:

  • Shampoos
  • Conditioners
  • Body washes
  • Lotions
  • Facial wipes

The company stated that it reported the issue voluntarily and is working closely with the FDA to resolve the matter. All affected deodorants were manufactured at the company’s Pennsylvania facility, which operates under FDA oversight.

What Should You Do if You Bought a Recalled Power Stick Product?

If you own any of the deodorants mentioned above, the FDA and A.P. Deauville strongly advise that you stop using them immediately.

Here’s what you can do:

✅ Step 1: Check the Lot Number

Locate the lot number printed on the bottle. If it matches any listed in this article, your deodorant is part of the recall.

✅ Step 2: Stop Using the Product

Even if you haven’t experienced any adverse effects, stop using the deodorant to avoid potential health risks associated with improperly manufactured products.

✅ Step 3: Contact the Company for Return or Refund

You can reach out to A.P. Deauville for instructions on how to return the product and obtain a refund or dispose of the product safely. Visit their official website or contact their customer service hotline.

Is This a One-Time Incident or a Broader Issue?

While A.P. Deauville has not faced widespread recalls in recent years, this incident raises concerns about manufacturing standards and oversight in the personal care industry. The company has pledged to reassess its procedures and ensure stricter compliance with FDA guidelines.

In recent times, the FDA has stepped up its vigilance over cosmetics and over-the-counter personal care products due to increasing scrutiny about safety, ingredient sourcing, and proper labeling.

What Is cGMP and Why Does It Matter?

The term cGMP stands for Current Good Manufacturing Practices, a system enforced by the FDA to ensure that products are consistently produced and controlled according to quality standards.

Violations can include:

  • Inadequate quality control
  • Improper sanitation
  • Incorrect labeling or packaging
  • Poorly trained staff
  • Substandard facility conditions

Products made outside these practices may not be safe, effective, or of acceptable quality.

FDA Proactively Recalls 67,000+ Cases of Power Stick Deodorant to Protect Consumer Safety

Stay Informed and Safe

This major recall of Power Stick deodorants is a clear reminder that even widely trusted and accessible personal care brands are not immune to safety oversights. While no direct injuries or contamination have been reported so far, the FDA and A.P. Deauville are taking preventive measures seriously.

As a consumer, the best thing you can do is:

  • Stay alert to FDA recall announcements
  • Double-check lot numbers on products
  • Follow return and refund instructions when needed

With responsible action and transparency from companies, recalls like this can help protect public health and maintain trust in essential everyday products.

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