FDA Announces Massive Deodorant Recall—Here's What to Look For It's still unclear what caused the recall. Close Credit: Kinga Krzeminska / Getty Images Key Points Over 67,000 cases of Power Stick antiperspirant deodorant have been recalled nationwide due to manufacturing issues.The recall stems from unspecified violations of Current Good Manufacturing Practices (cGMP), which are FDA-enforced standards to ensure product safety and consistency.The affected products were sold at major retailers including Walmart, Dollar Tree, and Amazon, prompting a wide-reaching consumer alert. Check the label on your deodorant ASAP. Tens of thousands of cases of Power Stick antiperspirant deodorant have been recalled due to an undisclosed manufacturing issue, according to the U.S. Food and Drug Administration (FDA). AP Deauville, manufacturer of personal care products, has launched a recall of 67,214 cases of its Power Stick antiperspirant deodorant. The products were distributed nationwide and sold at retailers such as Walmart and Dollar Tree and on Amazon. The affected products with their corresponding UPC codes and lot numbers include: Product Size UPC National Drug Code Lot Number Power Stick For Her Roll-on Antiperspirant Deodorant Powder Fresh 1.8 ounces 815195019313 42913-038-00 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402 Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spring Fresh 1.8 ounces 815195018194 42913-039-00 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391, 111626G231 Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant 1.8 ounces 815195018224 42913-040-00 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091, 111626G221 According to the FDA report, "cGMP deviations" are the reason for the recall, indicating that there was an inconsistency with the established procedures and standards outlined in the Current Good Manufacturing Practices (cGMP). The cGMP are a set of regulations enforced by the FDA that ensure the quality and safety of products, particularly in the pharmaceutical, food, and medical device industries. According to the FDA, "the regulations make sure that a product is safe for use, and that it has the ingredients and strength it claims to have." Current Good Manufacturing Practices (CGMP) deviations can occur at various stages of production, from raw material sourcing to finished product testing, and can range from minor errors to significant issues. The company did not disclose the specific deviation that initiated the recall. Explore more: News Recall News Related Articles Hand Sanitizers, Deodorants, and More Recalled Over Life-Threatening Contamination Risk Dog Food Recalled Due to Scary Health Risk to Pets and Humans—What to Know Popular Makeup Wipes Recalled Due to Bacteria Contamination—Check If Yours Are Affected First Aid Beauty Recalls 2,500 Jars of Cult-Favorite Moisturizer—Here's What to Know Massive Hair Dryer Recall Due to Electric Shock Risk—Here's What to Know Oysters and Clams Linked to Norovirus Outbreak Recalled Nationwide, FDA Warns Check Your Pantry: Nearly 200,000 Cans of Green Beans Recalled in 21 States Pancakes Recalled in 13 States Due to Allergy Risk—Here's What to Know Crackers Sold at Target, Walmart, and More Recalled Due to Metal Contamination—Here's What to Know Baby Powder Recalled Nationwide Due to Possible Asbestos Contamination Over 75,000 Bottles of Coffee Creamer Recalled Nationwide Due to Spoilage Concerns, Reports of Illness 2 Million Donuts and Pastries Recalled Nationwide Due to Listeria Risk, FDA Warns Over 150,000 Bottles of Water Recalled Due to Bacteria FDA Issues Urgent Recall for Canned Beef Stew Contaminated With Wood Fragments Chocolate Recall Considered Class I Due to 'Deadly' Allergen Risk, FDA Warns Broccoli Recall Considered Class I Due to 'Deadly' Listeria Risk, FDA Warns Newsletter Sign Up