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Power Stick Deodorant Recall: FDA Issues Alert for Over 67,000 Cases Due to Manufacturing Violations

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power stick deodorant recall
power stick deodorant recall

Key Takeaways:

  • The FDA has announced a recall of over 67,000 cases of Power Stick antiperspirant deodorant.
  • Affected products include Power Stick for Her, Invisible Protection, and Original Nourishing variants.
  • The recall was initiated due to cGMP (Current Good Manufacturing Practice) deviations, raising potential safety concerns.
  • Consumers are urged to check lot numbers and discontinue use of recalled products.

Power Stick Deodorant Recall: What You Need to Know

The U.S. Food and Drug Administration (FDA) has issued an enforcement report detailing a massive recall of Power Stick antiperspirant deodorant products. The recall, initiated by A.P. Deauville, affects over 67,000 cases of multiple Power Stick variants due to manufacturing violations.

This recall highlights potential risks associated with non-compliance with FDA’s Current Good Manufacturing Practice (cGMP) regulations, which ensure product safety and quality. Consumers who have purchased any of the affected products should immediately check the lot numbers and stop using them.

power stick deodorant recall
power stick deodorant recall

Which Power Stick Deodorant Products Are Recalled?

The recall includes the following Power Stick antiperspirant deodorant products:

  1. Power Stick for Her Roll-On Antiperspirant Deodorant (“Power Fresh” scent)
  2. Power Stick Invisible Protection Roll-On Antiperspirant Deodorant (“Spring Fresh” scent)
  3. Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant

Recalled Lot Numbers

The FDA enforcement report lists specific lot numbers for each recalled product:

1. Power Stick for Her Roll-On Antiperspirant Deodorant

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

2. Power Stick Invisible Protection Roll-On Antiperspirant Deodorant

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

3. Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant

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

Why Were These Power Stick Deodorants Recalled?

The FDA’s enforcement report cites “cGMP deviations” as the reason for the recall. Current Good Manufacturing Practices (cGMP) are strict regulatory standards that ensure products are consistently produced and controlled according to quality standards.

Possible concerns that may arise from cGMP violations include:

  • Contamination risks (bacterial or chemical)
  • Incorrect ingredient concentrations
  • Faulty packaging or labeling
  • Potential skin irritation or allergic reactions

While the FDA has not reported any specific injuries or adverse events linked to the recalled deodorants, the violation of manufacturing standards raises concerns about product safety.


What Should Consumers Do?

If you own any Power Stick deodorant products, take the following steps:

  1. Check the Lot Number – Locate the lot number on the packaging and compare it to the recalled batches listed above.
  2. Discontinue Use – If your product is part of the recall, stop using it immediately.
  3. Contact the Manufacturer – Reach out to A.P. Deauville or the retailer where you purchased the product for refund or replacement instructions.
  4. Monitor for Adverse Reactions – If you experience skin irritation, rashes, or allergic reactions, consult a healthcare professional.
  5. Report Issues to the FDA – Consumers can file a complaint via the FDA’s MedWatch Adverse Event Reporting program.

How to Stay Updated on the Power Stick Deodorant Recall

This is a developing story, and the FDA may release additional details. To stay informed:

  • Visit the FDA’s official recall page (www.fda.gov)
  • Check A.P. Deauville’s website for company announcements
  • Follow consumer safety alerts from trusted news sources

Final Thoughts

The Power Stick deodorant recall serves as a reminder of the importance of FDA compliance in personal care products. Consumers should always verify product recalls and take necessary precautions when using affected items.

If you have any of the recalled Power Stick deodorants, follow the recommended steps to ensure your safety. Stay tuned for further updates as this story develops.

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