425 recalls tagged with “burn risk”.
Baby Loren recalled children's loungewear on July 31, 2025, due to serious burn risks. The loungewear violates federal flammability standards, endangering children. Affected items include dresses in various prints and sizes 2T to 6Y.
Contract Medical International GmbH recalled 2,500 Fortress Introducer Sheath Systems on July 30, 2025. Units may have incorrect pouch labeling, leading to potential use of the wrong device version. Patients and healthcare providers should stop using the product immediately.
S.I.N. Implant System Ltda recalled 4,367 dental implants on July 30, 2025, due to improper storage conditions. The recalled products may have compromised packaging, affecting their quality and performance. Patients and healthcare providers should stop using these devices immediately.
ORTOMA AB recalled 261 Inserter Adapters on July 28, 2025, due to a potential weld failure. The defect poses a risk of improper positioning during hip implant procedures. The recall affects devices distributed worldwide, including the U.S. and countries like Japan and Sweden.
Medline Industries, LP recalled 596 medical convenience kits on July 25, 2025. The recall affects kits with Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to light failure. Patients and healthcare providers must stop using these devices immediately.
Medline Industries, LP recalled 2,520 medical convenience kits on July 25, 2025. The recall affects multiple intubation trays containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light in these devices fails to illuminate, posing a serious risk in emergency situations.
iMirror Inc. recalled its Electric Bug Zapper Racket, Fly Swatter, and Mosquito Swatter on July 24, 2025. The rechargeable battery can catch fire during extended use. Consumers should stop using the products and contact iMirror for a full refund.
FENGQS recalled F7 Pro electric bikes on July 24, 2025, due to fire hazards. The lithium-ion batteries can overheat and ignite, posing serious risks. Consumers should stop using the bikes immediately and seek refunds.
Curtis International recalled Frigidaire-brand minifridges on July 24, 2025. The recall affects models EFMIS129, EFMIS137, EFMIS149, and EFMIS175, due to fire and burn hazards. More than $700,000 in property damage has been reported.
Transpro US recalled electric scooters on July 24 due to fire hazards. The A3 Hub Motor, A11F Spark, and R1 Commuter scooters have unauthorized lithium-ion battery certification labels. Consumers should stop using these scooters and contact Transpro for a refund or replacement.
Winston Products recalled HydroTech 5/8-inch Expandable Burst-Proof Hoses on July 24, 2025. The hoses pose an impact hazard and risk of hearing impairment. Consumers should stop using the hoses and seek refunds immediately.
Bestway, Intex, and Polygroup recalled certain above-ground pools due to a drowning hazard. Nine deaths have been reported linked to this issue. The recall affects about five million pools sold since 2002.
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.
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.
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.
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.
North American Rescue recalled 552 Junctional Emergency Treatment Tools on July 1, 2025. The device may have a manufacturing defect that compromises its structural integrity. Healthcare providers should stop using it immediately and follow recall instructions.
Medtronic recalled 1,440 Simplera Sensors on May 7, 2025. The device cap label may not adhere properly, compromising sterility and increasing infection risk. Patients should stop using the device immediately and contact their healthcare provider for instructions.
CorNeat Vision recalled the CorNeat EverPatch surgical matrix on October 16, 2024. The recall affects the product's labeling for prevention and management of wound dehiscence. Distribution spans across the U.S. and several countries.