What Happened?

The U.S. Food and Drug Administration (FDA) announced a voluntary recall of over 67,000 cases of Power Stick roll-on deodorants sold at Walmart, Amazon, Dollar Tree, and other major retailers. The recall was triggered by cGMP (Current Good Manufacturing Practice) deviations, raising concerns over product quality and safety, despite no immediate health hazards reported.

Which Products Are Affected?

The recall covers three variants of Power Stick 1.8 oz (53mL) roll-on deodorants:

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

Affected lot codes are printed beneath the UPC barcode. If your product matches, discontinue use immediately.

Why Were They Recalled?

The FDA flagged cGMP deviations, meaning the deodorants were not manufactured under required quality standards. While there’s no evidence of contamination or health injuries, such deviations can compromise consistency, labeling, and overall safety.

What Should Consumers Do?

1. Check the lot code on your deodorant (found beneath the barcode).
2. Stop using the product if it matches recalled batches.
3. Return or dispose of the product — retailers like Walmart and Amazon are offering refunds.
4. Stay updated via the FDA Recall Page.

What Is cGMP and Why It Matters

Current Good Manufacturing Practices (cGMP) ensure consistent product quality, correct ingredient labeling, and contamination prevention. Any violation can affect consumer trust and safety, prompting preventive recalls like this one.

Resources & Further Reading