A significant nationwide recall has been initiated for more than 67,000 cases of Power Stick roll-on deodorants, impacting consumers across the United States. Manufacturer A.P. Deauville, based in Easton, Pennsylvania, voluntarily issued this extensive recall on July 10, 2025. The action follows concerns raised by the U.S. Food and Drug Administration (FDA) regarding the company’s manufacturing practices. These affected products were widely distributed and sold at major retailers, including popular chains like Walmart, Amazon, and Dollar Tree, making it crucial for a broad segment of the public to be aware. (cleveland.com, USA Today)
Understanding the Reason for Recall: cGMP Deviations
The primary reason cited for this recall is “cGMP deviations,” which refers to non-compliance with Current Good Manufacturing Practice regulations. These regulations, enforced by the FDA, are fundamental to ensuring the quality, safety, and efficacy of drug products, which include antiperspirants. cGMP provides a robust system of controls that govern the design, monitoring, and control of manufacturing processes and facilities. Adherence to these regulations is vital because it assures that products contain the ingredients and strength they claim to have, and are free from harmful contaminants or defects. While the FDA report indicated these deviations, the specific nature of the manufacturing issue that prompted the recall has not been publicly disclosed by A.P. Deauville or the FDA in most reports. A.P. Deauville did not immediately respond to requests for comment from several news outlets regarding the specifics of the defect. (CBS News, ABC News)
Identifying the Affected Products
The recall encompasses a combined total of 67,214 cases across three distinct Power Stick roll-on antiperspirant deodorant products, all packaged in 1.8 oz (53 mL) containers. Consumers are urged to carefully check their deodorant products for the following:
- Power Stick for Her Roll-on Antiperspirant Deodorant Powder Fresh: This variety accounts for 21,265 cases. Its UPC Code is 815195019313, and NDC# is 42913-038-00.
- Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spring Fresh: A total of 22,482 cases of this product are affected. Its UPC Code is 815195018194, and NDC# is 42913-039-00.
- Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant: This product has 23,467 cases under recall. Its UPC Code is 815195018224, and NDC# is 42913-040-00.
To ensure accurate identification, especially concerning specific production batches, consumers should refer to the comprehensive lists of lot numbers available on the official FDA enforcement report. Detailed information, including UPC, NDC, and specific lot numbers, can also be found in reports from news organizations such as KING5 and TODAY.com.
Consumer Action and Safety Recommendations
If you possess any of the recalled Power Stick roll-on deodorants, the FDA strongly advises that you immediately cease using the product and dispose of it. While the recall notice does not specify a remedy for consumers, some reports suggest that returning the product to the retailer where it was purchased may be an option. It is prudent to check all areas where you might store deodorant, including bathroom cabinets, gym bags, travel kits, and even your car, to ensure no affected products remain in use.
Product recalls, particularly for personal care items, underscore the continuous need for consumer vigilance. These measures are put in place to protect public health and safety. Staying informed about such announcements, whether through news outlets or directly via the FDA’s website, is paramount. For the most up-to-date information and any further guidance regarding this Power Stick deodorant recall, consumers are encouraged to visit the FDA’s official recall database.
