Latest news with #A.P.Deauville
Time of India
a day ago
- Health
- Time of India
FDA recall alert: Power Stick deodorants pulled from Walmart, Amazon over major manufacturing lapse — Is yours affected? Know here
The United States Food and Drug Administration (FDA) has just announced a mass recall of over 67,000 Power Stick deodorants. These deodorants were manufactured by A.P. Deauville, and the FDA had ordered their recall due to deviations from current good manufacturing practices, or cGMP. This Power Stick deodorant recall is voluntary, and the exact breakup of the deodorants being recalled is as follows: 21,265 cases of Power Stick for Her Roll-on Antiperspirant Deodorant Powder Fresh, 22,482 cases of Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spring Fresh, and 23,467 cases of Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant. The FDA recalled the Power Stick Deodorants for not following cGMP The Power Stick Deodorants were recalled because they didn't follow Current Good Manufacturing Practices. Complying with these practices is intended to ensure that 'a product is safe for use, and that it has the ingredients and strength it claims to have.', per the FDA's own website. A recall is underway for tens of thousands of cases of Power Stick antiperspirant deodorant, according to the Food and Drug Administration (FDA).An enforcement report published by the agency showed A.P. Deauville launched a recall for over 67,000 cases of "power fresh"-scented… The FDA is among the most crucial regulatory agencies in the United States, and its ambit covers everything from food safety to over-the-counter pharmaceutical drugs, alongside vaccines and cosmetics, and grooming products such as deodorants. The manufacturer of the recalled Power Stick Deodorants, A.P. Deauville, has not publicly spoken out about the recall. The Power Stick deodorants were sold at major retailers nationwide The recalled Power Stick Deodorants have been sold nationwide through various online and big box retail stores including Amazon, Walmart, and Dollar Tree. It's quite likely that these deodorants will have fallen into the hands of many Americans. Due to the voluntary nature of the recall, it remains unclear whether all of the 67,000 deodorant sticks will find their way back to the retailers. The FDA has generally recommended that consumers either return any products marked for recall or simply discard them. To stay updated on the stories that are going viral follow Indiatimes Trending.
Yahoo
a day ago
- Health
- Yahoo
FDA recalls over 67,000 cases of Power Stick deodorant due to manufacturing violations
Don't stop wearing deodorant, but it might be best to consider a new antiperspirant after a recent recall on Power Stick deodorants. On July 10, Pennsylvania-based health and beauty manufacturer A.P. Deauville announced a recall of 67,214 cases of its Power Stick roll-on deodorant due to violations of Current Good Manufacturing Practice (CGMP) standards, a set of FDA-enforced guidelines designed to ensure product safety and quality. The recall notice does not detail any consumer remedies or identify the specific regulatory violations involved. Here's what to know about the recalled deodorant. What deodorant products are being recalled? Where were the recalled products sold? According to the recall notice, the Power Stick deodorants were sold nationwide. The deodorants are available for purchase from major retailers such as Walmart and Amazon. What to do with the recalled Power Stick deodorant? The FDA recommends discarding recalled products or returning them to the retailer where the products were purchased, an FDA spokesperson told USA TODAY. -USA TODAY Network Greta Cross contributed to this report. This article originally appeared on Austin American-Statesman: FDA recalls Power Stick deodorant due to manufacturing violations Solve the daily Crossword
NBC News
2 days ago
- Health
- NBC News
More than 67,000 cases of Power Stick deodorant have been recalled — what to know
The Food and Drug Administration has issued a recall for more than 67,000 cases of Power Stick deodorant products for not meeting safety and quality standards. The antiperspirant deodorant items are made by A.P. Deauville, a company based in Easton, Pennsylvania. The following products have been recalled: 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 The items are being recalled for CGMP deviations. CGMP refers to Current Good Manufacturing Practices established by the FDA. 'CGMP provides for systems that assure proper design, monitoring, and control of manufacturing processes and facilities,' the FDA says on its website. 'Adherence to the CGMP regulations assures the identity, strength, quality, and purity of drug products by requiring that manufacturers of medications adequately control manufacturing operations.' 'This formal system of controls at a pharmaceutical company, if adequately put into practice, helps to prevent instances of contamination, mix-ups, deviations, failures, and errors,' the agency continued. Power Stick products are sold at Dollar Tree, Walmart and Amazon. The recall does not specify which regulations weren't adhered to, nor what consumers should do if they've already purchased these products. 'We take pride in manufacturing and offering products that are great quality at an affordable price,' A.P. Deauville says on its website. 'We obsess over every part of products from the color of the barrels to making sure the fragrances are on trend and last long. Our antiperspirant/deo sticks and shower products are manufactured in our FDA regulated factory.'
Arab Times
3 days ago
- Health
- Arab Times
FDA announces large-scale recall of popular deodorants
NEW YORK, July 20: The U.S. Food and Drug Administration (FDA) has announced a major recall involving tens of thousands of Power Stick deodorants produced by A.P. Deauville due to manufacturing defects. According to the agency, more than 67,000 cases of roll-on deodorants are affected by the recall, which was prompted by deviations from Current Good Manufacturing Practices (CGMP) — a set of industry standards that ensure quality and safety in pharmaceutical and personal care product manufacturing. The recalled items include: Power Stick for Her Roll-On Antiperspirant Deodorant Powder Fresh, 1.8 oz (53 mL)n Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spring Fresh, 1.8 oz (53 mL)n Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant Deodorant, 1.8 oz (53 mL)n The deodorants were distributed across the United States. Consumers are encouraged to check the FDA's website for specific lot numbers tied to the affected products. While no press release has been issued by A.P. Deauville at this time, the recall is ongoing, and the FDA continues to monitor the situation. 'Recalls are important because they protect the public from products that may cause injury, illness, or even death,' the FDA stated in its notice. The agency emphasizes that staying informed about product recalls is essential for consumer safety. Recalls can be initiated voluntarily by a manufacturer or at the request of the FDA. The agency notes that while many recalls result in products being pulled from the market, some issues can be corrected without removing products from distribution. Between 2014 and 2024, more than 83,000 FDA-regulated products were recalled in the U.S. For now, consumers in possession of the affected deodorants are advised to stop using them and refer to the FDA's recall database for next steps.
Time of India
3 days ago
- Health
- Time of India
Deodorant recalled: Why FDA recalled 67,000 cases of Power Stick deodorants sold at Walmart, Dollar Tree, and Amazon
After blueberries, Greek yogurt, chocolates, and even water bottles, the FDA is now recalling deodorants! The Food and Drug Administration (FDA) has issued a voluntary recall of over 67,000 cases of Power Stick roll‑on deodorants manufactured by A.P. Deauville. The recall, which was announced on July 10, covers three popular variants – Power Stick for Her 'Power Fresh', Invisible Protection 'Spring Fresh', and Original Nourishing Invisible Protection. These products were sold widely through Walmart, Dollar Tree, and Amazon, affecting consumers across the United States. The recall was reportedly triggered by deviations from the FDA's Current Good Manufacturing Practices (cGMP), a red flag for production oversight and quality control, although no contamination was reported. Read on to know more. What caused the recall? On July 10, A.P. Deauville initiated the recall of 67,214 combined cases of Power Stick deodorant sold nationwide. For the recall, the FDA enforcement reported cGMP deviations, which listed failures in adhering to current good manufacturing practices as the primary reason. The FDA strictly enforces cGMP regulations to ensure products are consistently produced with accurate ingredients, proper strength, and no contamination. by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like Do you have a mouse? Desert Order Undo These regulations ensure that products are consistently manufactured in controlled environments, maintaining quality, safety, and efficacy. However, it is important to note that no harmful substance was found in those products. cGMP issues, although do not always indicate direct harm, any breach in manufacturing protocols – be it equipment calibration, hygiene, ingredient verification, or documentation control – can compromise product integrity, making this recall a critical decision. Why cGMP compliance matters Current Good Manufacturing Practices (cGMP) form a regulatory backbone ensuring that mass‑produced items, from medications to deodorants, meet rigorous safety and quality benchmarks. When deviations occur, whether in cleanliness, equipment calibration, or ingredient testing, consumer safety can't be guaranteed, even if no immediate harm is reported. Even in the absence of direct harm, any cGMP lapse poses potential quality risks, hence the proactive recall. Which items were recalled The recall includes three 1.8-oz roll‑on deodorants, each with specific lot numbers: Power Stick for Her Roll‑On 'Power Fresh' – 21,265 cases, e.g., lots 032026B011, 071226D381, 082826E402. Power Stick Invisible Protection 'Spring Fresh' Roll‑On – 22,482 cases, e.g., 031726A991, 071026D361, 111626G231. Power Stick Original Nourishing Invisible Protection – 23,467 cases, e.g., 032826B221, 070626D301, 111626G221. These Power Stick variants were sold nationwide via: Walmart – 3‑packs sold at around $21 Dollar Tree – 24‑packs for about $30 Amazon – available as individual or multi‑packs Consumers who purchased from any of these retailers are urged to inspect the UPC/barcode on the packaging, match the lot numbers printed beneath to see if their purchase is affected, and discontinue use if their deodorant is part of the recall.
