1,030 recalls tagged with “electrical hazard”.
Medtronic recalled two units of the Octopus Nuvo Tissue Stabilizer on January 13, 2026, after identifying an assembly issue. The tubing was incorrectly positioned, posing a high hazard risk to patients. Healthcare providers and patients must stop using the device immediately to prevent potential complications.
Ford Motor Company recalled certain 2025 Explorer and Lincoln Aviator vehicles due to a rearview camera software defect. The rearview camera image may fail at speeds of 10 MPH or greater, increasing crash risk. Owners received notification letters on March 28, 2025.
FUJIFILM Healthcare Americas recalled 16 units of the CH-200 X-ray high-voltage generator on January 9, 2026. The electromagnetic contactors may weld, potentially causing overheating and smoke. The recall affects units distributed nationwide in various states including California and Florida.
Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.
Volkswagen Group of America recalled certain 2025 Tiguan vehicles due to a loose tie rod bolt. This condition may lead to a loss of vehicle control, increasing crash risk. Owner notification letters were mailed on September 5, 2025.
DR Power Equipment recalled walk-behind and tow-behind leaf vacuums after reports of laceration hazards. The recall affects multiple model numbers sold from September 2014 to June 2025. Consumers should stop using these vacuums immediately and seek repairs.
Isla Rae recalled magnetic wireless chargers on January 8, 2026, due to risks of fire and burn hazards. Consumers should stop using the chargers immediately and seek refunds. The chargers were sold at T.J. Maxx and Marshalls locations between June 2024 and November 2025.
Medline Industries recalled 150 dialysis convenience kits on January 8, 2026, due to silicone seal defects. Affected kits may obstruct fluid paths and risk exposure to biological contaminants.
Medline Industries recalled 14,525 dialysis convenience kits on January 8, 2026. The recall affects multiple product SKUs due to potential silicone seal failures. These issues may cause therapy delays or exposure to contaminants.
Medline Industries recalled 1,212 kits containing Tego Connectors on January 8, 2026. The recall stems from issues with silicone seals that may cause occluded fluid paths. Users may experience delays in therapy or exposure to contaminants due to this defect.
Medline Industries recalled 516 medical kits on January 8, 2026, due to issues with Tego Connectors. The silicone seal may tear or dome, posing a high risk of therapy interruption and exposure to contaminants. Healthcare providers must stop using these devices immediately and follow recall instructions.
Medline Industries recalled 2,020 dialysis kits on January 8, 2026, due to defective silicone seals. The seals may dome or tear, leading to fluid leaks and contamination. Patients and healthcare providers should stop using these kits immediately.
Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.
Medline Industries recalled 9,720 convenience kits on January 7, 2026, due to sterilization calibration issues. The affected products may not meet sterility assurance levels. Patients and healthcare providers should stop using these kits immediately.
Medline Industries, LP recalled 684 medical convenience kits on January 7, 2026. The recall affects the LVAD Driveline Tray and the KIT Surg Onc Insert Cent. Venou due to calibration issues impacting sterility. Health providers and patients should stop using these products immediately.
Olympus Corporation recalled 4,183 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. Devices may deform and lose performance due to inadequate thermoforming. Healthcare providers should immediately stop using the affected products and follow recall instructions.
Olympus Corporation of the Americas recalled 93 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to a manufacturing flaw. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 5,946 single use sphincterotomes on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must cease use immediately to avoid potential hazards.
Olympus Corporation recalled 1,474 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must stop using these instruments immediately.
Olympus Corporation of the Americas recalled 10,008 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to a manufacturing issue. Healthcare providers and patients must stop using them immediately.