Latest news with #PowerStickInvisibleProtectionRoll-OnAntiperspirantDeodorantSpringFresh
Time of India
2 hours 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.
Time of India
2 days ago
- Business
- Time of India
Over 67,000 cases of deodorants sold at Walmart, Amazon recalled due to 'cGMP deviations'. What is it?
Over 67,000 cases of three types of Power Stick deodorant sold at Walmart, Amazon and Dollar Tree have been recalled due to 'cGMP deviations". This means the product did not meet manufacturing regulations by the Food and Drug Administration (FDA). On Thursday, the US Food and Drug Administration announced a nationwide recall of some Power Stick deodorants , manufactured by A.P. Deauville . Explore courses from Top Institutes in Select a Course Category Degree Public Policy MCA Healthcare others Leadership Management Data Analytics Data Science Cybersecurity Digital Marketing Product Management healthcare Data Science PGDM Others Design Thinking CXO Finance MBA Technology Artificial Intelligence Operations Management Project Management Skills you'll gain: Data-Driven Decision-Making Strategic Leadership and Transformation Global Business Acumen Comprehensive Business Expertise Duration: 2 Years University of Western Australia UWA Global MBA Starts on Jun 28, 2024 Get Details The recall was voluntary and involves 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. by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like The Top 25 Most Beautiful Women In The World Articles Vally Undo ALSO READ: Astronomer CEO Andy Byron's divorce bill revealed following Coldplay kiss cam controversy with HR chief The FDA states that recall is due to 'cGMP deviations.' The agency's website notes that CGMP stands for 'Current Good Manufacturing Practice' and these regulations 'make sure that a product is safe for use, and that it has the ingredients and strength it claims to have.' Live Events The antiperspirants were distributed nationwide and sold at Walmart, Amazon and Dollar Tree. A.P. Deauville also makes shampoo, conditioner, lotion, body wash and facial wipes. What is CGMP? For the recall, the FDA enforcement reported cGMP deviations , which listed failures in adhering to current good manufacturing practices as the primary reason. According to FDA, the main regulatory standard for ensuring pharmaceutical quality is the Current Good Manufacturing Practice (CGMP) regulations for human pharmaceuticals. ALSO READ: Barron Trump 'humiliated' at NYU? Professor, peers make shocking statement about US President's son "CGMP refers to the Current Good Manufacturing Practice regulations enforced by the FDA. CGMP provides for systems that assure proper design, monitoring, and control of manufacturing processes and facilities. 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 includes establishing strong quality management systems, obtaining appropriate quality raw materials, establishing robust operating procedures, detecting and investigating product quality deviations, and maintaining reliable testing laboratories. 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. This assures that drug products meet their quality standards," FDA says. Why is CGMP so important? A consumer usually cannot detect (through smell, touch, or sight) that a drug product is safe or if it will work. While CGMP requires testing, testing alone is not adequate to ensure quality, the FDA says. In most instances testing is done on a small sample of a batch (for example, a drug manufacturer may test 100 tablets from a batch that contains 2 million tablets), so that most of the batch can be used for patients rather than destroyed by testing. ALSO READ: Shooting in Washington's Renton leaves 'multiple victims', police launch investigation Therefore, it is important that drugs are manufactured under conditions and practices required by the CGMP regulations to assure that quality is built into the design and manufacturing process at every step. However, it is important to note that no harmful substance was found in those products. "If a company is not complying with CGMP regulations, any drug it makes is considered 'adulterated' under the law. This kind of adulteration means that the drug was not manufactured under conditions that comply with CGMP. It does not mean that there is necessarily something wrong with the drug," according to FDA.
4 days ago
- Health
More than 67K cases of Power Stick deodorant products voluntarily recalled
More than 67,000 cases of roll-on deodorant that were sold nationwide have been voluntarily recalled due to an undisclosed manufacturing defect. A.P. Deauville, LLC, the manufacturer of Power Stick deodorants, initiated a voluntary recall for 67,214 combined total cases of three types of antiperspirant on July 10, 2025, according to a report from the U.S. Food and Drug Administration. The Pennsylvania-based manufacturer did not immediately respond to ABC News' request for comment. Details of deodorant recall The affected products include 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. All recalled items came in a 1.8-ounce package size. The reason for the recall, according to the FDA report, was "cGMP deviations," which indicates an issue with the established procedures and standards for how a product is made, as outlined in the Current Good Manufacturing Practices, or cGMP. As defined by the FDA, cGMP are a set of regulations to ensure product quality and safety. "The regulations make sure that a product is safe for use, and that it has the ingredients and strength it claims to have," the agency states on its website. Below, see the affected lot codes and product numbers to check if any deodorant labels may be in your home: Power Stick for Her Roll-On Antiperspirant Deodorant Powder Fresh: 1.8 oz/53 mL, UPC Code 815195019313, NDC# 42913-038-00, covering lots 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341 and 082826E402
The Hill
4 days ago
- Health
- The Hill
Deodorant sold by Walmart, Amazon recalled nationwide
(NewsNation) — Over 67,000 cases of three types of Power Stick deodorant have been recalled due to ' cGMP deviations,' meaning the product did not meet manufacturing regulations by the Food and Drug Administration (FDA). According to an FDA enforcement report, A.P. Deauville initiated the recall on July 10 for 67,214 cases of 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. The lot numbers of the recalled deodorant, according to the report, are: Power Stick for Her Roll-On: 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341 and 082826E402. Power Stick Invisible Protection Roll-On: 031726A991, 041226B561, 062026C901, 062026C911, 071026D351, 071026D361, 071326D391 and 111626G231. Power Stick Original Nourishing Invisible Protection Roll-On: 101225D781, 032926B281, 032826B221, 041126B531, 062226D011, 070626D301, 070626D333, 111026G051, 111326G091 and 111626G221. The antiperspirants were distributed nationwide and sold at Walmart, Amazon and Dollar Tree.
