1,030 recalls tagged with “electrical hazard”.
Philips North America recalled 1,913,441 IntelliVue MP80 monitors on October 31, 2025. The devices may fail to alarm, presenting a high risk to patient safety. Healthcare providers and patients should stop using the monitors immediately.
Polaris Industries recalled certain 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 ROVs due to a fire hazard. The recall affects vehicles sold between March 2025 and August 2025. Polaris urges consumers to stop using the recalled vehicles immediately.
Milwaukee Tool recalled M18 FUEL Top Handle Chainsaws due to a laceration hazard. The recall affects approximately 10,000 chainsaws sold since January 2023. Consumers should stop using the product immediately and contact Milwaukee Tool for a free repair.
Olympus Corporation of the Americas recalled 7,803 units of the HX-400U-30 ligating device on October 30, 2025. The device may fail to release as intended, posing significant risks to patients. Healthcare providers must stop using the device immediately and follow recall instructions.
B Braun Medical recalled 10,536 Anesthesia IV Sets on October 29, 2025. The recall stems from a risk of medication backflow between IV containers. Healthcare providers must stop using the product immediately to prevent potential harm.
B Braun Medical recalled 554,015 IV administration sets on October 29, 2025. The recall addresses a high risk of medication backflow into primary IV containers. Patients and healthcare providers must stop using these sets immediately.
B Braun Medical recalled over 49 million IV administration sets on October 29, 2025. The recall addresses a potential backflow of medication from secondary IV containers into primary IV containers. Users should stop using the affected devices immediately.
B Braun Medical recalled 33,528 blood administration sets on October 29, 2025. The recall affects sets used with Infusomat Space, Outlook, and Vista Basic Pumps. The devices pose a backflow risk that could compromise patient safety.
B Braun Medical recalled 162,648 IV administration sets on October 29, 2025. The products pose a high risk of backflow from secondary IV containers into primary containers. Affected sets include catalog number 354212, distributed worldwide.
B Braun Medical recalled 74,652 IV administration sets on October 29, 2025. The recall impacts users of the Infusomat Space, Outlook, and Vista Basic Pumps due to backflow risks. The affected catalog number is US9923F, with worldwide distribution including the US and Canada.
B Braun Medical recalled 46,250 IV administration sets on October 29, 2025. The recall follows concerns about potential backflow of medication into primary IV containers. The affected products were sold worldwide, including the US and Canada.
Medtronic recalled 6,591 extravascular implantable cardioverter defibrillators on October 29, 2025. The recall stems from a potential delay in high-voltage therapy that could occur under rare conditions. Patients must stop using the devices immediately and follow manufacturer instructions.
Philips North America recalled six units of the Incisive CT scanner on October 29, 2025, due to a serious safety hazard. The screws on the tube heat exchanger may not be properly tightened, leading to potential detachment during operation. This defect could cause damage to other components within the system.
Philips North America recalled 2,341 Incisive CT scanners on October 29, 2025. A component may detach and damage other parts during operation. Users must stop using the device immediately and follow recall instructions.
Medicrea recalled 44 units of its IB3D Universal Implant Inserter on October 29, 2025. The device's handle may untread from the shaft, preventing proper rotation of implants. The recall affects states including TN, CA, and TX.
B Braun Medical recalled 381,850 IV administration sets on October 29, 2025. The recall addresses potential backflow of medication from secondary IV containers into primary containers. This issue poses a significant risk to patients and healthcare providers worldwide.
B Braun Medical recalled 12,700 IV administration sets on October 29, 2025, due to a risk of medication backflow. The affected models include Catalog Number 352062, distributed worldwide including the US, Canada, and Germany. Healthcare providers must stop using these devices immediately.
B Braun Medical recalled 43,900 IV administration sets on October 29, 2025. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. Users must stop using these devices immediately due to a potential medication backflow hazard.
B Braun Medical recalled 5,448 blood administration sets on October 29, 2025. The recall affects devices used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The company cited potential backflow of medication and occlusion as the primary hazards.
B Braun Medical recalled 7,344 blood administration sets on October 29, 2025. The recall follows a potential backflow hazard that could affect patient safety. Healthcare providers must stop using the affected devices immediately.