The Recall Desk

State

Nebraska product recalls

73,741 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,580
Critical
713
Severe
1,345
Most recent
2026-10-28

Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.

Which agencies issued them

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38026–38050 of 78321

  • HighFDA (Devices)·Z-0698-2019·2019-01-16

    Ion Beam Applications Recalls Proteus 235 Proton Therapy Systems

    Ion Beam Applications is recalling seven Proteus 235 proton therapy systems due to a risk of detachment of the Compact Gantry Rolling Floor.

    Product
    Proteus 235 Product Usage: The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0376-2019·2019-01-16

    Lupin Recalls Cefdinir Oral Suspension Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension due to product complaints indicating the reconstituted suspension was observed to be thick.

    Product
    CEFDINIR — CEFDINIR (CEFDINIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0693-2019·2019-01-16

    GE Healthcare Recalls MRI Systems Due to Possible Incorrect Software Version

    GE Healthcare is recalling 3,849 MRI systems worldwide because they may have an incorrect software version loaded.

    Product
    Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for general diagnostic use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0707-2019·2019-01-16

    Siemens Biograph Horizon PET/CT System Recalled for Design Defects

    Siemens Medical Solutions USA is recalling 171 Biograph Horizon PET/CT systems worldwide due to improper design or specifications.

    Product
    Siemens Biograph Horizon PET/CT System, Product Usage: The Siemens Biograph systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0375-2019·2019-01-16

    Lupin Recalls Cefdinir Oral Suspension Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension because product complaints indicated the reconstituted suspension was observed to be thick.

    Product
    CEFDINIR — CEFDINIR (CEFDINIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V018000·2019-01-15

    Chrysler Recalls Vehicles Due to Exploding Passenger Air Bag Inflator Risk

    Chrysler is recalling specific 2010-2016 Dodge, Chrysler, and Jeep vehicles because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    CHRYSLER — CHRYSLER, DODGE, JEEP 300, CHARGER, CHALLENGER, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V015000·2019-01-14

    BMW Recalls 2000-2004 Models for Air Bag Inflator Explosion Risk

    BMW is recalling specific 2000-2004 5 Series and X5 vehicles because the air bag inflator in optional sports steering wheels may explode, posing a serious injury risk.

    Product
    BMW — BMW 540I, 525I, X5 SAV, 530I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V016000·2019-01-14

    BMW Recalls 2015 X1 Vehicles for Driver Air Bag Inflator Defect

    BMW is recalling 2015 X1 vehicles because the driver's air bag inflator may explode due to humidity, posing a risk of serious injury or death.

    Product
    BMW — BMW X1 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V017000·2019-01-14

    BMW Recalls X5 and X6 Models Due to Air Bag Inflator Defect

    BMW is recalling 2007-2014 X5 and X6 models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW X5, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V032000·2019-01-14

    Volvo Recalls 2018-2019 VNL Trucks for Clutch Assembly Defect

    Volvo is recalling 2018-2019 VNL trucks with automated manual transmissions because a clutch component may fail, causing unintended vehicle movement.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V031000·2019-01-14

    Ford Recalls 2019 Lincoln Nautilus for Lane Center Assist Defect

    Ford is recalling 2019 Lincoln Nautilus vehicles because the Lane Center Assist system may fail to detect if the driver's hands are off the steering wheel for a prolonged period.

    Product
    LINCOLN — LINCOLN NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V014000·2019-01-11

    Volkswagen and Audi Recall Vehicles Due to Airbag Inflator Defect

    Volkswagen is recalling specific 2015-2017 models because the driver's airbag inflator may explode during deployment, potentially causing serious injury.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI EOS, PASSAT, CC, TT ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V029000·2019-01-11

    Double K Recalls 2017-2018 Hometown Trolley Buses for Brake Bolt Issue

    Double K is recalling 2017-2018 Hometown Trolley buses because loose brake caliper bolts may reduce braking effectiveness and increase crash risk.

    Product
    HOMETOWN TROLLEY — HOMETOWN TROLLEY STREETCAR, MAINSTREET, VILLAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V030000·2019-01-11

    Double K Recalls 2017-2019 Hometown Trolley Buses for Brake Bolt Issue

    Double K is recalling 2017-2019 Hometown Trolley buses because brake caliper bolts may loosen, reducing brake effectiveness and increasing crash risk.

    Product
    HOMETOWN TROLLEY — HOMETOWN TROLLEY STREETCAR, VILLAGER, MAINSTREET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·19V008000·2019-01-09

    Subaru Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Subaru is recalling specific 2010-2014 models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU OUTBACK, FORESTER, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·19V010000·2019-01-09

    Mercedes-Benz Recalls Vehicles Due to Passenger Air Bag Inflator Defect

    Mercedes-Benz is recalling specific 2010-2017 models because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C300, E350, GLK350, C350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0552-2019·2019-01-09

    Medtronic StealthStation Cranial Software Recall for Biopsy Depth Gauge Error

    Medtronic is recalling StealthStation Cranial and Synergy Cranial software due to an incorrect display of the Biopsy Depth Gauge that resulted in the biopsy of healthy tissue.

    Product
    StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for cranial procedures using optical localization StealthStation Cranial version 3.0, 3.1 CE 0344 Rx Only 2018-02 9735489 Revision 3 Medtronic Navigation, Inc.…
    Category
    Medical Device
    Distribution
    51 states
  • SevereNHTSA·19V005000·2019-01-09

    Toyota Recalls Vehicles for Front Passenger Air Bag Inflator Defect

    Toyota is recalling approximately 1.3 million vehicles because front passenger air bag inflators may explode due to humidity, potentially causing serious injury or death.

    Product
    LEXUS — LEXUS, TOYOTA, SCION IS F, COROLLA, COROLLA MATRIX, 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V009000·2019-01-09

    Subaru Recalls Vehicles Due to Air Bag Inflator Explosion Risk

    Subaru is recalling specific 2010-2014 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU OUTBACK, FORESTER, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V007000·2019-01-09

    Subaru Recalls Vehicles Due to Front Passenger Air Bag Inflator Defect

    Subaru is recalling specific 2010-2014 models because front passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU OUTBACK, FORESTER, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V006000·2019-01-09

    Ferrari Recalls Multiple Models Due to Passenger Air Bag Inflator Defect

    Ferrari is recalling various models from 2014 to 2018 because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    FERRARI — FERRARI CALIFORNIA T, FF, F12 BERLINETTA, 488 GTB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0688-2019·2019-01-09

    Ortho-Clinical Diagnostics Recalls VITROS HBeAg Reagent Due to Biased Results

    Ortho-Clinical Diagnostics is extending a 2018 recall of VITROS HBeAg Reagent because biotin interference may cause inaccurate test results.

    Product
    VITROS HBeAg Reagent, Cat. No 6801819 Product Usage: For the in vitro qualitative detection of hepatitis B e antigen (HBeAg) in human adult and pediatric (2 to 21 years old) serum from individuals who have symptoms of hepatitis or who may be at risk for hepatitis B virus…
    Category
    Medical Device
    Distribution
    Distributed nationwide