Hazard
116 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 116 power loss recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 29 (25%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all power loss recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Medtronic MiniMed is recalling 83,398 MiniMed 780G insulin pumps distributed throughout the United States due to battery cap deterioration that may cause power loss and device malfunction.
Medtronic MiniMed is recalling the MiniMed 630G insulin pump due to battery cap deterioration that may cause loss of power and function. Approximately 126,558 units distributed in the U.S. and Canada are affected.
Medtronic has recalled approximately 323,417 MiniMed 640G insulin pumps due to battery cap deterioration that may cause loss of power and functionality. Patients should contact Medtronic or their healthcare provider immediately.
Medtronic recalls certain MiniMed 740G Insulin Pumps due to battery cap deterioration that may cause loss of power and functionality. No illnesses have been reported.
Medtronic MiniMed is recalling approximately 575 MiniMed 720G Insulin Pumps due to battery cap deterioration that may result in power loss and device malfunction.
Subaru is recalling certain 2020-2021 Outback and Legacy vehicles for a transmission control unit programming error that may cause the drive chain to slip, resulting in loss of drive power and increased crash risk.
GE Healthcare recalls backup batteries for anesthesia devices worldwide that may fail earlier than expected. The batteries are used in Avance CS2, Avance, Amingo, and Aespire View systems.
Invacare TDX SP2 power wheelchairs may experience battery harness disconnection during shipment or use, resulting in loss of power. Approximately 133 affected devices have been distributed in the U.S. and Canada.
Chrysler is recalling 2021 Jeep Grand Cherokee and Dodge Durango vehicles due to EGR valve defects that may cause loss of drive power and increase crash risk. Dealers will provide free replacement.
Ford is recalling 2022 Lincoln Aviator PHEV vehicles. The inlet charge port harness bus bar may unseat, causing loss of drive power and increasing crash risk.
General Motors is recalling 2021-2022 Chevrolet Corvette vehicles whose rear half-shaft assemblies may be missing ball bearings. This can cause sudden loss of drive power, increasing crash risk.
Braun recalls 2020-2021 Chevrolet Traverse wheelchair vehicles for a transmission fluid leak hazard. A faulty screw and clip may cause fluid loss, risking power loss, crashes, and fire.
Toyota is recalling 2022 Prius and Prius Prime vehicles whose Engine Control Unit software may falsely trigger shutdown of the hybrid system, causing loss of drive power. Contact Toyota at 1-800-331-4331 for a free software update.
Certain 2020-2021 Land Rover Discovery vehicles have a loose battery ground contact causing electrical failure and potential vehicle shutdown while driving. Dealers will replace the ground stud at no cost.
Arcimoto is recalling 2019-2021 FUV, 2020 Deliverator, 2020-2021 Roadster, and 2021 Rapid Responder vehicles due to a software error that may cause unexpected battery shutdown, increasing crash risk. Owners should contact Arcimoto or NHTSA for remedy details.
INFINITI is recalling 2021 Q50 and Q60 vehicles for an Engine Control Module software defect that may cause engine stall and increase crash risk. Dealers will reprogram the ECM software free of charge.
Respironics is recalling 2,144 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.
Respironics is recalling 835 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.
Respironics is recalling 3,453 V680 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Respironics is recalling 934 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Respironics is recalling 292 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Respironics is recalling 3,213 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Respironics is recalling 534 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.
Respironics is recalling 702 V60 Plus Ventilators worldwide because the backup battery may fail if over-discharged or stored without AC power.
Respironics is recalling 481 V60 Ventilators due to potential backup battery failures caused by over-discharge or extended storage without AC power.