Browse through 2,234 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
DJO Surgical recalled 447 units of the Altivate Reverse Wedge Glenoid Reamer Sleeve on July 18, 2025. The recall follows reports that the device may kick or bind during use, presenting a serious hazard to patients. Healthcare providers and patients should discontinue use immediately and follow the manufacturer's instructions.
DJO Surgical recalled 907 units of the Altivate Reverse Wedge Glenoid Reamer on July 18, 2025, due to a kickback risk during use. The recall affects healthcare providers and patients nationwide across 25 states. This Class II recall warns of potential binding issues that could lead to serious injury.
DJO Surgical recalled 439 AltiVate Reverse Glenoid Trays on July 18, 2025, due to potential reamer malfunction. The reamer may kick or bind during use, posing a serious risk to patients. Healthcare providers should stop using the device immediately and follow the recall instructions.
DJO Surgical recalled 927 units of the Altivate Reverse Wedge Glenoid Reamer Head on July 18, 2025. The recall follows reports that the device may kick or bind up during use. Healthcare providers and patients must stop using the product immediately.
DermaRite Industries LLC recalled 249 bottles of DermaSarra External Analgesic on July 17, 2025. The product contains camphor and is contaminated with Burkholderia cepacia. This recall is classified as Class I due to the potential health risks.
DermaRite Industries recalled 5,703 bottles of PeriGiene antiseptic on July 17, 2025. The product contains Burkholderia cepacia, posing health risks. Consumers must stop using the product immediately.
C.R. Bard recalled 3,670 Foley catheter trays on July 17, 2025, due to incorrect inserts. Users may confuse materials, leading to allergies or infections. Healthcare providers and patients must stop using these trays immediately.
iStore recalled 5,000 Magnetic Wireless Power Banks on July 17, 2025. The recall affects model IST-09991/W05 due to overheating and fire hazards. Consumers should stop using the devices immediately and seek a refund.
Deale International recalled CasaClean Handheld Steamers on July 17, 2025, due to a burn injury hazard. The recall affects model DF-958, sold at HSN from November 2024 through April 2025 for about $40. Users should stop using the product immediately and follow refund instructions.
Babyletto recalled its Kiwi Electronic Recliner on July 17, 2025, due to a fire hazard. The USB module can overheat and spark, posing a risk to users. Consumers should stop using the recliners immediately and contact Babyletto for a repair kit.
Tractor Supply recalled multiple models of its Traveller aluminum loading ramps on July 17, 2025. These ramps can bend or break under weight, posing a fall hazard. Consumers should stop using them immediately and seek refunds.
C.R. Bard recalled 4,300 Foley catheter trays on July 17, 2025. Incorrect inserts may lead users to misidentify materials, increasing infection and allergic reaction risks. Patients and healthcare providers must stop using the trays immediately and follow recall instructions.
VIVI recalled lithium-ion batteries for e-bikes on July 17, 2025. The batteries can overheat, posing fire and burn hazards. Consumers must stop using the affected e-bikes immediately.
Primark recalled DTR Stitch Scented Highlighters on July 17, 2025, due to phthalate exposure. The highlighters, resembling slushie containers, pose a health risk to children. Consumers should stop using them immediately and seek a refund.
C.R. Bard Inc issued a recall for 4,300 Foley catheter trays on July 17, 2025. Incorrect inserts lead to potential allergic reactions and infection risk. Healthcare providers and patients must stop using the device immediately.
Quest International recalled 376 Measles IgM Test Kits on July 17, 2025. The kits lack premarket approval or clearance from the FDA. Healthcare providers and patients must stop using these kits immediately.
DermaRite Industries recalled 6,973 cartridges of KleenFoam Antimicrobial Foam Soap on July 17, 2025. The product contains a harmful bacterial contamination, Burkholderia cepacia. Consumers should stop using the soap immediately and seek guidance from healthcare providers.
DermaRite Industries LLC recalled 11,321 bags of DermaKleen antiseptic lotion soap on July 17, 2025. The product, contaminated with Burkholderia cepacia, poses a serious health risk. Consumers should stop using the product immediately and contact health providers for guidance.
Stryker Communications recalled 40 surgical light systems on July 15, 2025, due to potential powder coating chipping. This defect increases risks for healthcare providers and patients. Affected products were distributed nationwide, including Texas, Illinois, and New York.
AUGNORYE recalled padded crib bumpers on July 10, 2025, after reports of suffocation hazards. The bumpers violate federal safety regulations. Consumers should stop using them immediately and request a refund.