The Recall Desk

State

Nebraska product recalls

73,806 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.

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43151–43175 of 78386

  • ModerateFDA (Devices)·Z-0305-2018·2018-01-10

    Zimmer Biomet Recalls Distal Femoral Knee Implant Due to Labeling Error

    Zimmer Biomet is recalling a specific lot of distal femoral knee implant assemblies because the internal patient label may be incorrect, although the product itself is correctly identified.

    Product
    RED SEXP DSTL FEM 19CM LT ASSY, model # CP111828
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0296-2018·2018-01-10

    Zimmer Biomet Recalls Lateral Troch Plate Due to Labeling Error

    Zimmer Biomet is recalling Lateral Troch Plate Full Crimp units because the internal patient label may be incorrect, though the product itself is correct.

    Product
    Lateral Troch Plate Full Crimp - 254mm, model # 350837
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0314-2018·2018-01-10

    Smiths Medical Medfusion Syringe Infusion Pump Recall for Clamp Loosening

    Smiths Medical is recalling Medfusion Syringe Infusion Pumps because a loose clamp mechanism may cause the device to incorrectly alarm for invalid syringe sizes.

    Product
    Medfusion, Syringe Infusion Pump, Software Version 6 (V6), Rx Only, Manufactured by Smiths Medical ASD, Inc., 1500 Eureka Park, Lower Pemberton, Ashford, Kent, TN25 4BF, UK. In the administration of fluids requiring precisely controlled infusion rates including blood or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0301-2018·2018-01-10

    Zimmer Biomet Recalls CER OPTION TYPE 1 TPR SLEVE -6 Due to Labeling Error

    Zimmer Biomet is recalling CER OPTION TYPE 1 TPR SLEVE -6 devices because the internal patient label may be incorrect, although the outer box and product are correctly identified.

    Product
    CER OPTION TYPE 1 TPR SLEVE -6, model # 650-1064
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0306-2018·2018-01-10

    Euro Diagnostica Recalls DIASTAT ANA ELISA Kits Due to Performance Deviation

    Euro Diagnostica is recalling 534 DIASTAT ANA ELISA kits (Lot TS 2076) distributed in Minnesota, Nebraska, and Texas because a component deviation may cause false positive results.

    Product
    Euro Diagnostica DIASTAT ANA (anti-nuclear antibody) ELISA DIASTAT ANA (anti-nuclear antibody) A positive ANA test result provides presumptive evidence for systemic rheumatic disease; further definition of specific antibody profiles is a valuable aid in the diagnostic…
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0297-2018·2018-01-10

    Zimmer Biomet Recalls Lateral Troch Plate Due to Labeling Error

    Zimmer Biomet is recalling Lateral Troch Plate Full Crimp devices because the internal patient label may be incorrect, although the outer box and product are correctly identified.

    Product
    Lateral Troch Plate Full Crimp - 254mm, model # 350838
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0299-2018·2018-01-10

    Zimmer Biomet Recalls COMP Primary Stem Due to Labeling Error

    Zimmer Biomet is recalling COMP Primary Stem 8MM MINI devices because the internal patient label may be incorrect, although the product itself is correctly identified.

    Product
    COMP PRIMARY STEM 8MM MINI, model # 113628
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V031000·2018-01-09

    Tesla Recalls 2013 Model S Vehicles Due to Air Bag Inflator Defect

    Tesla is recalling 17,846 2013 Model S vehicles because the passenger frontal air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V021000·2018-01-09

    Chrysler, Dodge, and Ram Vehicles Recalled for Air Bag Inflator Defect

    Chrysler is recalling specific 2009-2013 vehicles because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    DODGE — DODGE, JEEP, CHRYSLER CHALLENGER, DAKOTA, WRANGLER, 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V014000·2018-01-09

    Subaru Recalls 2009 Models Due to Air Bag Inflator Explosion Risk

    Subaru is recalling 2009 Forester, Legacy, Impreza, Tribeca, WRX, and Outback vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU FORESTER, LEGACY, IMPREZA, TRIBECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V030000·2018-01-09

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

    BMW is recalling 2007-2013 X5 and 2009-2013 X6 vehicles because the 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·18V016000·2018-01-09

    Mazda Recalls 2009 B-Series Trucks Due to Air Bag Inflator Defect

    Mazda is recalling 2009 B-Series trucks because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V018000·2018-01-09

    Mazda Recalls CX-7, Mazda6, and CX-9 for Air Bag Inflator Defect

    Mazda is recalling 2009-2013 CX-7, Mazda6, and CX-9 vehicles because the front passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA CX-7, MAZDA6, CX-9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V040000·2018-01-09

    Ferrari Recalls 2013 Models Due to Air Bag Inflator Explosion Risk

    Ferrari is recalling 1,899 2013 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    FERRARI — FERRARI 458, CALIFORNIA, FF, F12 BERLINETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V012000·2018-01-09

    Subaru Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Subaru is recalling specific 2009-2013 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU FORESTER, LEGACY, IMPREZA, TRIBECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V041000·2018-01-09

    Honda Recalls Acura RL, Element, and Ridgeline for Air Bag Defect

    Honda is recalling specific 2009-2013 Acura RL, Honda Element, and Ridgeline vehicles because the passenger air bag inflator may explode, posing a risk of serious injury or death.

    Product
    ACURA — ACURA, HONDA RL, RIDGELINE, ELEMENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V013000·2018-01-09

    Subaru Recalls 2009-2010 Models for Air Bag Inflator Defect

    Subaru is recalling 2009-2010 vehicles in 22 states because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU FORESTER, LEGACY, IMPREZA, TRIBECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V024000·2018-01-09

    Toyota Recalls Lexus, Scion, and Toyota Vehicles for Airbag Defect

    Toyota is recalling specific 2009-2013 Lexus, Scion, Toyota, and Pontiac vehicles because the passenger airbag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    LEXUS — LEXUS, SCION, TOYOTA IS 350C, IS 350, IS 250C, IS 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V056000·2018-01-09

    E-One Emergency Vehicles Recalled for Electrical Fire Risk

    E-One is recalling 2005-2010 emergency vehicles because loose electrical connections at the transfer switch may cause excessive heat and increase the risk of a fire.

    Product
    E-ONE — E-ONE CYCLONE III, CYCLONE II, TYPHOON, F550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V025000·2018-01-09

    Toyota Recalls Yaris, Vibe, and Corolla Matrix for Air Bag Defect

    Toyota is recalling 116,126 vehicles due to a defect in passenger frontal air bag inflators that may explode during deployment, posing a risk of serious injury or death.

    Product
    PONTIAC — PONTIAC, TOYOTA VIBE, YARIS, COROLLA MATRIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V032000·2018-01-09

    2013 Freightliner and Mercedes-Benz Sprinter Passenger Air Bag Recall

    Daimler Vans USA is recalling 2013 Sprinter vans because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V020000·2018-01-09

    New Flyer Transit Buses Recalled for Air Brake Hose Tightness Issue

    New Flyer is recalling 283 transit buses because improperly tightened air brake hoses may disconnect, increasing braking distance and crash risk.

    Product
    NEW FLYER — NEW FLYER XT60, XN40, XDE60, XDE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V042000·2018-01-09

    Honda Recalls Vehicles for Air Bag Inflator Explosion Risk

    Honda is recalling specific 2009-2013 models because the passenger air bag inflator may explode, potentially causing serious injury or death.

    Product
    HONDA — HONDA, ACURA FIT EV, CIVIC HYBRID, CIVIC, ACCORD CROSSTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide