The Recall Desk

State

Nebraska product recalls

72,919 recalls have nationwide distribution and so reach Nebraska. 4,547 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,547
Critical
705
Severe
1,119
Most recent
2026-09-09

Of the 4,547 recalls naming Nebraska we have scored against our rubric, 705 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,119 (25%) are Severe.

These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2676–2700 of 77466

  • LowFDA (Devices)·Z-1619-2026·2026-04-01

    Philips C9-4 ultrasound transducer labelling updated to define useful life

    Philips is recalling one C9-4 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips C9-4 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1626-2026·2026-04-01

    Philips S5-2 ultrasound transducer labelling updated to define useful life

    Philips is recalling one S5-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips S5-2 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1621-2026·2026-04-01

    Philips L17-5 ultrasound transducer labelling updated to define useful life

    Philips is recalling two L17-5 Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips L17-5 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1623-2026·2026-04-01

    Philips OMNI II TEE transducer labelling updated to define useful life

    Philips is recalling two OMNI II TEE Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips OMNI II TEE Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1627-2026·2026-04-01

    Philips X3-1 ultrasound transducer labelling updated to define useful life

    Philips is recalling the X3-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips X3-1 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1625-2026·2026-04-01

    Philips S4-1 ultrasound transducer labelling updated to define useful life

    Philips is recalling the S4-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips S4-1 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1618-2026·2026-04-01

    Philips 3D6-2 ultrasound transducer labelling updated to define useful life

    Philips is recalling the 3D6-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips 3D6-2 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1628-2026·2026-04-01

    Philips X7-2 ultrasound transducer labelling updated to define useful life

    Philips is recalling the X7-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips X7-2 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1624-2026·2026-04-01

    Philips OMNI III TEE transducer labelling updated to define useful life

    Philips is recalling the OMNI III TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips OMNI III TEE Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1622-2026·2026-04-01

    Philips Mini Multi TEE transducer labelling updated to define useful life

    Philips is recalling the Mini Multi TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips Mini Multi TEE Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V205000·2026-03-31

    2026 Ford Explorer and Mustang Engine Piston Circlip Defect Recall

    Ford is recalling certain 2026 Explorer and Mustang vehicles because engine piston circlips may have been incorrectly installed, risking loss of drive power and increasing crash risk.

    Product
    FORD — FORD EXPLORER, MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V201000·2026-03-31

    2025–2026 Ford Bronco Sport and Maverick Occupant Sensor Recall

    Ford is recalling certain 2025–2026 Bronco Sport and Maverick vehicles because the front passenger occupant classification sensor may fail to detect a passenger, risking failure of the airbag to deploy in a crash.

    Product
    FORD — FORD MAVERICK, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V202000·2026-03-31

    Ford Recalls 2026 Explorer and Aviator for HVAC Defrost Failure

    Ford is recalling 2026 Lincoln Aviator and Explorer vehicles because the HVAC system may fail, causing the windshield defrosting and defogging systems to become inoperative.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V206000·2026-03-31

    Nova Bus Recalls 2024-2025 LFS Models Due to Window Glass Detachment Risk

    Nova Bus is recalling 2024 LFS Artic and 2025 LFS transit buses because inadequate window frame adhesion may cause glass to detach, increasing injury and road hazard risks.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V204000·2026-03-31

    Ford and Lincoln windshield wiper arms may break causing wiper failure

    Ford is recalling certain 2021-2023 Lincoln Navigator, Expedition and Super Duty vehicles because the windshield wiper arms may break, causing the wipers to fail.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR, F-250 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V203000·2026-03-31

    Toyota Corolla Cross Hybrid may not sound sufficient pedestrian warning

    Toyota is recalling certain 2023-2025 Corolla Cross Hybrid vehicles because they may fail to make sufficient pedestrian warning sounds when in reverse. This fails FMVSS 141.

    Product
    TOYOTA — TOYOTA COROLLA CROSS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V200000·2026-03-29

    Aston Martin DBX rear lower suspension arm may crack or shear

    Aston Martin is recalling certain 2021-2026 DBX, DBX707 and DBX S vehicles because the torque reaction link pin may slide out of the rear lower suspension arm, cracking or shearing the arm casting.

    Product
    ASTON MARTIN — ASTON MARTIN DBX, DBX S, DBX707
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V196000·2026-03-27

    KTM 390 electronic throttle control may fail after water entry

    KTM is recalling certain 2022-2023 390 Duke and 2022-2024 RC 390 motorcycles because water may enter the electronic throttle control unit and cause it to fail, losing drive power while riding.

    Product
    KTM — KTM RC 390, 390 DUKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V198000·2026-03-27

    Mercedes-Benz Recalls 2025 G 580 EV Due to Incorrect Wheel Bolts

    Mercedes-Benz is recalling 2025 G 580 EVs because incorrect wheel bolts may have been installed, posing a risk of wheel detachment and crashes.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 580 EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V199000·2026-03-27

    2026 Mercedes-Benz GLE and GLS models air bag deployment failure recall

    Mercedes-Benz is recalling certain 2026 GLE and GLS models because the passenger air bag fabric may have been manufactured incorrectly, preventing proper deployment during a crash and increasing injury risk.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ, MERCEDES-MAYBACH GLE 580 4MATIC, GLE 350 4MATIC, GLE 450 4MATIC, GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E015000·2026-03-27

    Luxfer Recalls Unified Fine Pitch Thread Adapters Due to Fire Risk

    Luxfer Canada Ltd. is recalling specific Unified Fine Pitch thread adapters because an incompatible O-ring recess may cause hydrogen leaks and fire.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide