FDA Recalls Deodorant
FDA Recalls Over 67,000 Cases of Power Stick Deodorant Due to Manufacturing Violations
July 21, 2025 – The U.S. Food and Drug Administration (FDA) has announced a nationwide recall of more than 67,000 cases of Power Stick deodorants due to deviations from Current Good Manufacturing Practice (CGMP) standards. The recall affects three types of roll-on antiperspirant deodorants sold at major retailers, including Walmart, Amazon, and Dollar Tree. Consumers are advised to stop using the recalled products immediately and either dispose of them or return them to the place of purchase for a refund.
📋 Details of the Recalled Products 📋
Consumers should verify their deodorant against these lot numbers and UPC codes to determine if their product is part of the recall. The affected products were distributed nationwide and sold at major retailers, including Walmart, Amazon, and Dollar Tree.
⚠️ Reason for the Recall ⚠️
The recall was triggered by “cGMP deviations,” referring to violations of the FDA’s Current Good Manufacturing Practice regulations. These regulations ensure that products are consistently produced and controlled according to quality standards, covering aspects such as manufacturing processes, facilities, equipment, and testing. According to the FDA, CGMP compliance ensures that a product is safe for use and contains the ingredients and strength it claims to have.
The specific nature of the manufacturing violations has not been disclosed by either A.P. Deauville or the FDA. Such deviations could potentially affect the safety, identity, strength, quality, or purity of the deodorants, though no injuries have been reported in connection with this recall. The voluntary recall reflects a precautionary approach to protect consumer safety.
🛠️ Consumer Actions 🛠️
The FDA advises consumers who have purchased the recalled Power Stick deodorants to take the following steps:
- Stop Using the Product: Discontinue use of the deodorant immediately to avoid potential risks.
- Check Lot Numbers: Compare the lot numbers and UPC codes on your product with those listed above.
- Dispose or Return: Either discard the product or return it to the retailer where it was purchased for a refund.
- Seek Further Information: For questions or concerns, contact the FDA or the manufacturer.
No injuries or adverse effects have been reported, but the FDA urges consumers to act promptly out of caution.
🧠 Background on CGMP Regulations 🧠
Current Good Manufacturing Practice (CGMP) regulations are a cornerstone of the FDA’s oversight of products like cosmetics, including deodorants. These standards require manufacturers to maintain rigorous controls over their production processes to ensure product safety and efficacy. According to the FDA, “CGMP provides for systems that assure proper design, monitoring, and control of manufacturing processes and facilities.” Violations, such as those leading to this recall, could involve issues like contamination, improper labeling, or inconsistencies in product formulation.
While the exact violations in this case remain undisclosed, the recall underscores the importance of adhering to these standards to protect public health. The FDA’s enforcement of CGMP regulations helps prevent issues that could compromise product safety or effectiveness.
🏭 About Power Stick and A.P. Deauville 🏭
Power Stick deodorants are produced by A.P. Deauville, a health and beauty product manufacturer based in Easton, Pennsylvania. The brand is known for its affordable antiperspirant deodorants, widely available at major retailers. This recall appears to be a significant event for the brand, as no previous recalls of Power Stick products have been widely reported.
A.P. Deauville has not issued a press release regarding the recall, and the company has not responded to requests for comment from multiple news outlets. The FDA’s recall notice remains the primary source of information for consumers.
ℹ️ How to Stay Informed ℹ️
Consumers seeking additional details about the recall can visit the FDA’s official recalls page or contact the FDA directly. To report any issues with FDA-regulated products, including adverse reactions, use the FDA’s reporting system.
🌐 Broader Context of Product Recalls 🌐
The FDA defines a recall as an action taken by a company to remove or correct a product that violates U.S. regulations or poses a potential health risk. Recalls are classified based on the level of hazard, ranging from Class I (most severe) to Class III (least severe). The classification for this Power Stick recall has not been specified, but the absence of reported injuries suggests it may be a lower-risk issue. The FDA’s recall database, available for three years before archiving, provides a resource for tracking such actions.
This recall highlights the critical role of regulatory oversight in ensuring consumer safety. As products like deodorants are used daily by millions, adherence to manufacturing standards is essential to prevent potential risks.
🏁 Conclusion 🏁
The recall of over 67,000 cases of Power Stick deodorants is a significant action to protect consumers from potential risks associated with manufacturing violations. While the specific issues remain undisclosed, the FDA’s guidance is clear: stop using the affected products and take appropriate action. Consumers are encouraged to stay informed through official FDA channels and to check their products carefully.
TI GET MORE INFORMATION VISIT :https://fintechzoom-insights.com
❓ Frequently Asked Questions (FAQs) ❓
Q: Which Power Stick deodorants are affected by the recall?
A: The recall includes three types of Power Stick roll-on antiperspirant deodorants in 1.8 oz/53 mL packages: Power Stick for Her Powder Fresh, Invisible Protection Spring Fresh, and Original Nourishing Invisible Protection. Check the UPC codes and lot numbers listed above to confirm if your product is affected.
Q: Why were these deodorants recalled?
A: The recall was initiated due to violations of the FDA’s Current Good Manufacturing Practice (CGMP) standards, which could affect the safety or quality of the products. Specific details about the violations have not been disclosed.
Q: Have any injuries been reported?
A: No injuries or adverse effects have been reported in connection with the recalled deodorants, but the recall is a precautionary measure.
Q: What should I do if I have a recalled product?
A: Stop using the product immediately. You can either dispose of it or return it to the retailer (e.g., Walmart, Amazon, or Dollar Tree) for a refund.
Q: Where can I get more information about the recall?
A: Visit the FDA’s official recalls page or contact the FDA for further details.
Q: Are other Power Stick products safe to use?
A: The recall only applies to the specific products and lot numbers listed. Other Power Stick products are not currently affected, but check the FDA’s website for updates.
