The Recall Desk

State

Nebraska product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48901–48925 of 78397

  • HighNHTSA·16V842000·2016-11-21

    Hyundai Recalls Tucson and Santa Fe for Trailer Hitch Wiring Defect

    Hyundai is recalling 2016-2017 Tucson and 2017 Santa Fe vehicles because a trailer hitch wiring malfunction may cause brake lights to stay on, confusing other drivers.

    Product
    HYUNDAI — HYUNDAI TUCSON, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V843000·2016-11-21

    Hyundai Recalls 2007-2008 Entourage Vehicles for Hood Latch Defect

    Hyundai is recalling 2007-2008 Entourage vehicles because the secondary hood latch may corrode and fail to engage, increasing crash risk if the hood opens while driving.

    Product
    HYUNDAI — HYUNDAI ENTOURAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V836000·2016-11-18

    Volvo Bus Recalls 9700 Models Due to Engine Stall Risk

    Volvo Bus is recalling 2008-2017 9700 buses because an undersized power feed relay may fail, causing the engine to stall and increasing crash risk.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V838000·2016-11-18

    Navistar Recalls IC Bus CE and BE Models for Heater Hose Defect

    Navistar is recalling 157 IC Bus CE and BE transit buses because a heater hose may split, leaking hot coolant into the driver's foot area.

    Product
    IC BUS — IC BUS CE, BE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V839000·2016-11-18

    Maserati Recalls 2017 Models for Backup Camera Software Defect

    Maserati is recalling 7,481 model year 2017 Quattroporte, Ghibli, and Levante vehicles because the backup camera may disable in freezing temperatures, increasing crash risk.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI, LEVANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V837000·2016-11-18

    Navistar Recalls IC Bus School Buses Due to Heater Hose Defect

    Navistar is recalling specific IC Bus school buses because a heater hose may split, leaking hot coolant into the driver's foot area and increasing the risk of burns or crashes.

    Product
    IC BUS — IC BUS CESB, CASB, CE, BE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V831000·2016-11-17

    Mercedes-Benz Recalls 2017 E-Class Vehicles for Underbody Fire Risk

    Mercedes-Benz is recalling 799 model year 2017 E400 and E550 vehicles because insufficient clearance between the catalytic converter and underbody panel may cause a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E550, E400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V832000·2016-11-17

    BMW Recalls 2011 5-Series Vehicles for Air Bag Sensor Defect

    BMW is recalling 2011 528i, 535i, and 550i models because a replacement sensor unit may be incorrectly programmed, potentially preventing air bags and safety features from deploying in a crash.

    Product
    BMW — BMW 535I, 550I, 528I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V834000·2016-11-17

    Thor Motor Coach Recalls 2014-2016 Tuscany Motorhomes for Fire Risk

    Thor Motor Coach is recalling 528 Tuscany motorhomes because water leaks into the keyless entry module, causing electrical shorts that increase fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0352-2017·2016-11-16

    Hershey Recalls SoFit Protein Plus Sunflower Seeds Due to Listeria Risk

    The Hershey Company is voluntarily recalling SoFit Protein Plus Sunflower Seeds because a supplier expanded its recall for potential Listeria monocytogenes contamination.

    Product
    SOFiT Protein Plus Sunflower Seeds Sea Salt; Seeds covered by a crunchy protein shell: NET WT. 1 OZ.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0354-2017·2016-11-16

    Hershey Recalls SoFit Protein Plus Pumpkin Seeds Due to Listeria Risk

    The Hershey Company is voluntarily recalling SoFit Protein Plus Pumpkin Seeds Sesame Garlic because a supplier expanded its recall of sunflower seeds, creating a potential Listeria monocytogenes contamination risk.

    Product
    SOFiT Protein Plus Pumpkin Seeds Sesame Garlic, Seeds covered by a crunchy protein shell: NET WT. 1 OZ.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0308-2017·2016-11-16

    Ev3 Neurovascular Alligator Retrieval Device Recalled for Coating Defect

    Micro Therapeutics Inc. is recalling 3,337 Alligator Retrieval Devices because the PTFE coating may delaminate and detach, potentially entering the bloodstream.

    Product
    Alligator Retrieval Device The device is intended for use in the peripheral and neurovasculature for foreign body removal. Catalog No. FA-88810-20V04 FA-88810-20V06 FA-88810-30V04 FA-88810-30V06 FA-88810-40V04 FA-88810-40V06 FA-88810-50V04 FA-88810-50V06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0353-2017·2016-11-16

    Hershey Recalls SoFit Protein Plus Almonds Due to Listeria Risk

    The Hershey Company is voluntarily recalling SoFit Protein Plus Almonds Jalapeno Garlic because a supplier expanded its recall of sunflower seeds, creating a potential Listeria monocytogenes contamination risk.

    Product
    SOFiT Protein Plus Almonds Jalapeno Garlic, whole almonds covered by a crunchy protein shell: NET WT. 1 OZ.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0307-2017·2016-11-16

    FDA Recalls Pipeline Embolization Devices Due to Coating Delamination

    Micro Therapeutics Inc is recalling Pipeline Embolization Devices because PTFE coating may delaminate and enter the bloodstream.

    Product
    Pipeline Embolization Device (Pipeline Classic) The device is indicated for the endovascular treatment of adults (22 year of age or older) with large or giant widenecked intracranial aneurysms (lAs) in the internal carotid artery from the petrous to the superior hypophyseal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0310-2017·2016-11-16

    Ev3 Neurovascular Recalls X-Celerator Hydrophilic Exchange Guidewires

    Micro Therapeutics Inc is recalling X-Celerator Hydrophilic Exchange Guidewires because PTFE coating delamination may release material into the bloodstream.

    Product
    X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300 103-0601-350V10 103-0602-350V06 103-0601-300V01 103-0602-300 103-0602-350V09 103-0601-300V02 103-0602-300V01 103-0602-350V10 103-0601-300V03 103-0602-300V02 103-0601-300V06 103-0602-300v06…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0328-2017·2016-11-16

    SentreHeart Recalls FindrWIRZ Guidewire Systems Due to Coating Defects

    SentreHeart Inc is recalling FindrWIRZ Guidewire Systems because the lubricious coating delaminated and flaked off three units in Germany.

    Product
    FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended for use in the cardiovascular system for introduction and positioning of over the-wire catheters and therapeutic devices during interventional procedures.
    Category
    Medical Device
    Distribution
    15 states
  • SevereFDA (Food)·F-0351-2017·2016-11-16

    Professional Botanicals Recalls MealPlex and Pearl Drinks for Undeclared Milk

    Professional Botanicals is recalling specific lots of MealPlex and Pearl meal drinks because they contain undeclared milk, a major food allergen.

    Product
    Professional Botanicals MealPlex (756 grams) and Veo Natural Pearl 3.0 (378 grams) Ultimate Meal Drinks in Plastic Tub Containers. Dietary Supplement.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0374-2017·2016-11-16

    Siemens SOMATOM Definition Flash CT Systems Recalled for Injury Risk

    Siemens is recalling 57 SOMATOM Definition Flash CT systems in the US due to a hardware issue that may expose users to rotating or electrical parts.

    Product
    SOMATOM Definition Flash system, x-ray, tomography, computed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0373-2017·2016-11-16

    Siemens SOMATOM Definition AS CT Systems Recalled for Injury Risk

    Siemens Medical Solutions is recalling 57 SOMATOM Definition AS CT systems due to a hardware issue that may expose users to rotating or electrical parts.

    Product
    SOMATOM Definition AS system, x-ray, tomography, computed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0325-2017·2016-11-16

    On the Border Tortilla Chips Recalled for Possible Metal Fragments

    Truco Enterprises is recalling On the Border Cafe Style Tortilla Chips due to possible metal fragments in the corn flour.

    Product
    On the Border Cafe Style Tortilla Chips 18 oz. and 28 oz. packaged in laminated polypropylene film with windows.
    Category
    Food
    Distribution
    Distributed nationwide