1,120 recalls tagged with “electrical hazard”.
BMW recalls 2025 motorcycles with optional eCall system due to a software error that can deactivate emergency crash notification. OTA or dealer update will fix the issue. Letters to owners go out Sept. 12, 2025. Contact BMW at 1-800-525-7417.
Medline Industries, LP recalled 2,520 Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles sold to U.S. hospitals and healthcare facilities. The lights on the handles may fail to illuminate as intended. Hospitals should stop using the devices immediately and follow recall instructions.
Medline Industries, LP recalled 596 Medline kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light may fail to illuminate as designed. Healthcare providers should stop using the devices immediately and follow recall instructions.
Quallent Pharmaceuticals Health LLC recalls 1,856 bottles of Duloxetine delayed-release capsules due to CGMP deviations and an impurity above FDA interim limits. The recall is active as of August 20, 2025. Patients and providers should stop use and contact Breckenridge Pharmaceutical or a healthcare provider for guidance.
Zap Surgical Systems recalled 17 ZAP-X Radiosurgery System units worldwide, including US states FL, CO, NJ, NY and several countries. A software defect could cause the collimator to collide with patient shoulders or the patient table during long gantry moves after proximity errors. Clinicians and patients should stop using the device and follow recall instructions from the manufacturer.
Minongad recalled LED Gloves model ST01 after safety violations exposed battery ingestion risk. The recall covers gloves sold on Amazon with two pre-installed lithium coin batteries and four spare batteries. Consumers should stop using the gloves immediately and return them for a full refund.
Hyundai Motor America recalls 2025 IONIQ 5 vehicles due to a potentially loose bus bar in the high voltage battery system. The recall covers 2025 IONIQ 5 models. Hyundai says a short circuit could cause a fire. Owners should park outside away from structures until the remedy is complete and contact Hyundai at 1-855-371-9460. The recall number is 280.
Apollo recalled 2,000 Apollo City 2024 electric scooters sold by Apollo. A weld-line crack can cause the stem to break, creating fall and injury hazards. Owners should stop riding immediately and contact Apollo for a free stem replacement.
Transpro US recalls three scooter models sold with unauthorized lithium-ion battery UL certification labels. The recall covers A3 Hub Motor, A11F Spark, and R1 Commuter scooters. Consumers should stop using these scooters immediately and contact Transpro for a refund or replacement.
Curtis International Ltd. recalled Frigidaire-brand minifridges sold nationwide after more than $700,000 in property damage was reported. Internal electrical components can short circuit and ignite the surrounding plastic housing. Consumers should stop using recalled units immediately and contact Curtis for a full refund.
Innovative Designs recalled Minecraft Light-Up Slap Ruler Bracelets sold at retailers due to a button cell battery ingestion hazard. The recall covers models 718508MCR and 718075MCR. Consumers should stop using the recalled bracelets immediately and email disposal photos to info@innovativenyc.com to receive a full refund.
FENGQS recalled F7 Pro electric bikes with batteries produced on 2024-04-21. The bikes were sold blue and marketed under the FENGQS name. The lithium-ion battery can overheat and ignite, creating a fire and burn risk. Consumers should stop using the recalled bikes immediately and contact FENGQS for a full refund.
iMirror Inc. recalls Electric Bug Zapper Racket, Fly Swatter and Mosquito Swatter sold on Amazon and at imirror.com on July 24, 2025. The recall cites a hazard where the rechargeable battery can catch fire with extended use. Consumers should stop using the products immediately and contact iMirror for a full refund.
BMW of North America recalls 2022–2025 i4, 2022–2024 iX, 2023–2024 i7, and 2024 i5 vehicles over software that may shut down the high-voltage system, causing loss of drive power. OTA software updates or dealer service will fix the issue at no cost. Letters to owners begin August 5, 2025.
Ascend Laboratories recalls 8,568 bottles of Amlodipine and Olmesartan Medoxomil tablets due to failed dissolution specifications. The recall covers products manufactured by Alkem Laboratories in India and distributed nationwide in the USA. The defect involves low dissolution results. Stop use immediately and contact Ascend Laboratories for guidance.
Summa Therapeutics recalled 22 units of the Finesse BTK Multicath Injectable Angioplasty Balloon Catheter sold to healthcare facilities in New Jersey and Florida. The balloon may not meet burst specifications, raising risk during angioplasty. Healthcare providers must stop using the device immediately and follow recall instructions from Summa Therapeutics.
DJO Surgical recalled 927 ALTIVATE reverse wedge glenoid reamer heads distributed nationwide in the United States after concerns that the devices may kick or bind up during use. The issue involves model 804-06-311 and non-sterile stainless steel material. Healthcare providers and patients should stop using the device immediately and contact Encore Medical, LP for instructions.
DJO Surgical recalled 907 units of the ALTIVATE reverse wedge glenoid reamer boss drill 6.5mm sold nationwide in the United States. The device may kick or bind up during use. Healthcare providers and patients should stop using the device immediately and follow recall instructions from Encore Medical, LP.
DJO Surgical is recalling 447 ALTIVATE Reverse Glenoid Reamer Sleeve devices distributed nationwide in the United States. The device may kick or bind up during or immediately prior to use. Healthcare providers and patients should stop using the device and follow recall instructions issued by Encore Medical, LP via email.
DJO Surgical recall affects 439 AltiVate Reverse Glenoid Tray kits distributed across 26 states and Puerto Rico. A reamer in the kit may kick or bind during use. Patients and clinicians should stop using the device and follow manufacturer instructions.