A major recall of popular deodorants sold nationwide has been issued the second-highest risk classification by the U.S. Food and Drug Administration (FDA).
The recall of three Power Stick deodorants, affecting more than 67,000 products sold across the United States, was voluntary issued by Pennsylvania-based maker A.P. Deauville on July 10. FDA inspectors classified the recall a Class II on July 31.
The deodorants sold at retailers, including Dollar Tree and Amazon, are: Power Stick for Her Roll-On Antiperspirant Deodorant (Powder Fresh), Power Stick Invisible Protection Roll-On Antiperspirant Deodorant (Spring Fresh), and Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant (Original).
Newsweek contacted the company for comment on July 17.
Why It Matters
The recall signaled that the recalled Power Stick products were linked to violations of Current Good Manufacturing Practice (CGMP) requirements, which are intended to ensure drug products are produced under quality systems that assure identity, strength, quality and purity.
A recall is designated Class II status, the second highest of three, in situations where use “may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote,” the FDA says.
A.P. Deauville is also a manufacturer of shampoos, conditioners, lotion, body washes and facial wipes.
In 2005, the company’s Power Stick product also had a $50,000 settlement with the California Air Resources Board based on accusations that products contained volatile organic compounds beyond the state limit.
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What To Know
The recall covered the three antiperspirants with the following lot numbers:
- Power Stick for Her Roll-On Antiperspirant Deodorant Powder Fresh, 1.8 oz/ 53 mL UPC Code 815195019313—(21,265 cases)
- Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spring Fresh, 1.8 oz/53 mL UPC Code 815195018194—(22,482 Cases)
- Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant, 1.8 oz/53 mL UPC Code 815195018224—(23,467 Cases)
Consumers are urged to top using the products and follow retailer or manufacturer guidance for returns or disposal.
The FDA identified “CGMP deviations” as the reason for the recall but did not specify which regulations were not met.
What People Are Saying
Manufacturer A.P. Deauville, per its website: “Our antiperspirant/deo sticks and shower products are manufactured in our FDA regulated factory. We could save money ‘outsourcing’ or not caring enough to make it ourselves, but we CHOOSE to own our factory and make our product. With those savings, we can have the best quality and ensure you can afford our great products.”
What Happens Next?
The FDA’s enforcement report listed the recalls as ongoing.