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https://www.cpsc.gov/Recalls/2022/Acme-United-Corporation-Recalls-PhysiciansCare-Brand-Over-the-Counter-Drugs-Due-to-...
Submission: On March 20 via manual from US — Scanned from DE
Submission: On March 20 via manual from US — Scanned from DE
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Skip to main content United States Consumer Product Safety Commission * Recalls * Business Education * News Releases * Regulatory Robot * Calendar Events * Multimedia En | Es | 汉字 * Current Selected Language English Menu * Recalls * Business Education * News Releases * Regulatory Robot * Calendar Events * Multimedia En | Es | 汉字 * Safety Education * Safety Education Resources * Safety Education Materials Library * Neighborhood Safety Network * Community Outreach Center * Recall App * Business and Manufacturing * Business and Manufacturing Resources * Testing & Certification * Regulatory Robot * Recall Guidance * Small Business Assistance * Import Resources * International * Open Government * CPSC Data * Recall API * Section 6(b) Information Disclosure * Laws, Regulations, and Proceedings * Regulations, Laws & Standards * Statutes * Voluntary Standards * Legislative Affairs * Notices of Violations * Rulemaking * Adjudicative Proceedings * Research and Reports * Research and Reports Overview * Agency Reports * Clearinghouse Online Query Tool * NEISS Injury Statistics * About Us * About CPSC * Chair * Commissioners * Consumer Ombudsman * Office of Inspector General * Office of Equal Employment Opportunity and Minority Enterprise * Office of Communications * Office of the Secretary * Freedom of Information Act * Employment Information * Consumer Opinion Surveys * Division of Field Operations * Archive * Contact Us SearchSearch * Current Selected Language English ACME UNITED CORPORATION RECALLS PHYSICIANSCARE BRAND OVER-THE-COUNTER DRUGS DUE TO FAILURE TO MEET CHILD RESISTANT PACKAGING REQUIREMENT; RISK OF POISONING (RECALL ALERT) * * SHARE: * Share it on Facebook * Share it on Twitter * Copy Link * Copy link * Recalled PhysiciansCare Extra Strength Non Aspirin in 50 Tablets (25 Packets, 2 tablets each) * Recalled PhysiciansCare Aspirin in 250 Tablets (125 Packets, 2 tablets each) * Recalled PhysiciansCare Extra Strength Pain Reliever in 250 Tablets (125 Packets, 2 tablets each) * Recalled PhysiciansCare Ibuprofen in 500 Tablets (250 Packets, 2 tablets each) * Recalled PhysiciansCare Medication Station with outer station includes Ibuprofen, Extra Strength Non Aspirin, Antacid and Aspirin in 50 Tablets (25 Packets, 2 tablets each) * Recalled PhysiciansCare Multi-Pack without outer station includes Extra Strength Non Aspirin, Aspirin, Ibuprofen and Antacid in 50 Tablets (25 Packets, 2 tablets each) * Front of PhysiciansCare Aspirin packet * Back of PhysiciansCare Aspirin packet * Previous * Next * * * * * * * * * Previous * Next Name of Product: PhysiciansCare brand Aspirin, Extra Strength Non Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack Hazard: The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) which must be in child resistant packaging when being used in the household as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children. Remedy: Refund Recall Date: March 17, 2022 Units: About 165,000 Consumer Contact Acme United toll-free at 888-520-2199 from 8 a.m. to 5 p.m. ET, Monday through Friday, or online at www.recallrtr.com/acmeunitedotc or at www.acmeunited.com and click on “Recalls” at the bottom of the page for more information. RECALL DETAILS Description: This recall involves the PhysiciansCare brand Extra Strength Non Aspirin, Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack over-the-counter drugs. The products contain aspirin, acetaminophen, or ibuprofen. They are packaged in cardboard boxes of 50, 100, 250, and 500 tablets per box. Product Drug Tablet Amount Extra Strength Non Aspirin Acetaminophen (500 mg) 50 tablets 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Aspirin Aspirin (325 mg) 50 tablets 100 tablets 250 tablets 500 tablets Extra Strength Pain Reliever Acetaminophen (250 mg) Aspirin (250 mg) 100 tablets 250 tablets Ibuprofen Ibuprofen (200 mg) 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Medication Station / Multi-Pack Acetaminophen (500 mg) Aspirin (325 mg) Ibuprofen (200 mg) Antacid (420 mg) 4 boxes of 100 tablets each with outer station 4 boxes of 100 tablets each without outer station The Antacid is not subject to this recall. Remedy: Consumers should immediately store the recalled products in a safe location out of reach of children and contact Acme United for information on how to dispose of or return the product and receive a full refund. Acme United is contacting all purchasers directly. Incidents/Injuries: None reported Sold At: Amazon.com and FSAstore.com from February 2014 through June 2021 for between $5 and $50. Manufacturer(s): Acme United of Rocky Mount, North Carolina and Acme United of Vancouver, Washington Manufactured In: United States Recall number: 22-733 Choose Your Recall Emails Get Notified About Each Recall via Email. RELATED RECALLS HD Premier Recalls DigitDots Magnetic Balls Due to Ingestion Hazard When two or more high-powered magnets are swallowed, either intentionally by younger children or accidentally by older children, the ingested magnets can attract to each other, or to another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death. Acme United Corporation Recalls PhysiciansCare Brand Over-the-Counter Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert) The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) which must be in child resistant packaging when being used in the household as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children. B. toys Walk ‘n’ Learn Wooden Activity Toddler Walkers Recalled Due to Choking Hazard; Distributed by Maison Battat The wheels and wheel attachment hardware can detach from the walker in small pieces, posing a choking hazard to young children. Crate and Barrel Recalls Be the Band Music Sets Due to Choking and Suffocation Hazards The maracas can break or become unscrewed and release the metal beads inside, posing choking and suffocation hazards to young children. Bebe au Lait Recalls Teethers Due to Choking Hazard The string that connects the beads on the teethers can come untied, releasing the beads and posing a choking hazard to young children. TJX Recalls Menorahs Due to Fire Hazard; Sold at Marshalls, HomeGoods and Homesense Stores The resin and medium-density fiberboard (“MDF”) menorahs can burn or catch fire when holding lit candles, posing a fire hazard. * Search Product Safety Reports * About Government Recalls * Recalls from around the world About the U.S. CPSC The U.S. Consumer Product Safety Commission (CPSC) is charged with protecting the public from unreasonable risks of injury or death associated with the use of thousands of types of consumer products. Deaths, injuries, and property damage from consumer product incidents cost the nation more than $1 trillion annually. CPSC’s work to ensure the safety of consumer products has contributed to a decline in the rate of deaths and injuries associated with consumer products over the past 40 years. Federal law bars any person from selling products subject to a publicly announced voluntary recall by a manufacturer or a mandatory recall ordered by the Commission. For lifesaving information: * Visit CPSC.gov. * Sign up to receive our e-mail alerts. * Follow us on Facebook, Instagram @USCPSC and Twitter @USCPSC. * Report a dangerous product or a product-related injury on www.SaferProducts.gov. * Call CPSC’s Hotline at 800-638-2772 (TTY 301-595-7054). * Contact a media specialist. 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