The Recall Desk

State

Nebraska product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31051–31075 of 78302

  • LowFDA (Devices)·Z-1909-2020·2020-05-13

    Gentell Honey Hydrogel Saturated Gauze Recalled for FDA Registration Failure

    Gentell, Inc. is recalling 4,348 units of Gentell Honey Hydrogel Saturated Gauze because the product was not properly registered with the FDA.

    Product
    Gentell Honey Hydrogel 4"x8" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number: GEN-11830 - Product Usage: Use Gentell Honey Hydrogel on wounds with little or no exudate, diabetic skin ulcers, venous stasis ulcers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1907-2020·2020-05-13

    Gentell Honey Hydrogel Gauze Recalled for FDA Registration Failure

    Gentell, Inc. is recalling 85,586 units of Gentell Honey Hydrogel 2"x2" Saturated Gauze because the product was not properly registered with the FDA.

    Product
    Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number:GEN-11230 - Product Usage: Use Gentell Honey Hydrogel on wounds with little or no exudate, diabetic skin ulcers, venous stasis ulcers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1849-2020·2020-05-13

    Epimed RF Injector Cannula Recalled for Incorrect Expiration Date

    Epimed International is recalling 1,374 units of RF Injector Cannulas due to incorrect expiration dates on the packaging.

    Product
    R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 - Product Usage: The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V266000·2020-05-12

    Blue Bird Recalls School Buses Due to Air Conditioner Fire Risk

    Blue Bird is recalling 2020-2021 Vision and All American school buses because an incorrectly installed air conditioning circuit breaker may increase the risk of a fire.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V267000·2020-05-12

    Blue Bird Recalls 2020-2021 Transit Buses for A/C Fire Risk

    Blue Bird is recalling 2020-2021 Vision and All American buses because an incorrectly installed air conditioning circuit breaker may increase the risk of a fire.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, ALL AMERICAN TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V258000·2020-05-08

    Blue Bird Recalls 2020-2021 School Buses for Parking Brake Assembly Defect

    Blue Bird is recalling 2020-2021 Vision and All American school buses because the foot pedal parking brake assembly may be improperly assembled, potentially failing to hold the vehicle on an incline.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V261000·2020-05-08

    Maintainer Recalls 2019-2020 International and Chevrolet Tow Vehicles for PTO Defect

    Maintainer is recalling 16 modified 2019-2020 International CV and Chevrolet Silverado tow vehicles because incorrectly installed Power Take Offs may loosen, risking transmission fluid loss and rear wheel lockup.

    Product
    INTERNATIONAL — INTERNATIONAL, INTERNATIONAL MOTORS CV, CHEVY SILVERADO MEDIUM DUTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V259000·2020-05-08

    Blue Bird Recalls 2020-2021 Vision and All American Transit Buses

    Blue Bird is recalling 2020-2021 Vision and 2021 All American buses because the parking brake may fail to hold the vehicle on an incline.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, ALL AMERICAN TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V262000·2020-05-08

    Ford Recalls 2020 Expedition and Navigator for Pre-Collision Assist Defect

    Ford is recalling 2020 Expedition and Lincoln Navigator vehicles because the Pre-Collision Assist feature is not enabled due to incorrect coding, increasing crash risk.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V263000·2020-05-08

    Ford Recalls 2019-2020 Mustang and 2019 Expedition for Warning Defect

    Ford is recalling 2019-2020 Mustang and 2019 Expedition vehicles because the 'Transmission Not In Park' warning is shorter than intended, which may increase the risk of unintended vehicle movement.

    Product
    FORD — FORD MUSTANG, EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E030000·2020-05-08

    McNeilus Recalls CNG Fuel Systems with Defective Pressure Relief Devices

    McNeilus is recalling certain CNG fuel systems sold as aftermarket parts because the pressure relief devices may fail to vent during heat exposure, potentially causing the system to rupture.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:PRESSURE RELIEF DEVICES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V255000·2020-05-07

    Navistar Recalls 2018-2020 International Trucks Due to Engine Defect

    Navistar is recalling 2018-2020 International LT and 2019-2020 RH trucks because a wrist pin bushing failure may cause unexpected engine shutdown and increase crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL LT, RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V254000·2020-05-07

    GM Recalls 2015-2016 Chevrolet SS and Caprice for Steering Defect

    General Motors is recalling 2,281 vehicles due to potential loss of electric power steering assist caused by connector corrosion.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS, CAPRICE POLICE PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20741·2020-05-07

    Sobeauty Recalls Mag Cube Magnetic Ball Sets Due to Ingestion Risk

    Sobeauty is recalling Mag Cube magnetic ball sets because the small, high-powered magnets pose a serious risk of intestinal injury or death if swallowed by children.

    Product
    Mag Cube magnetic ball sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20119·2020-05-07

    Noah Clothing Recalls Men's Reverse Fleece Hoodies for Burn Hazard

    Noah Clothing is recalling men's reverse fleece hoodies because they fail federal flammability standards, posing a burn risk. No injuries have been reported.

    Product
    Noah Reverse Fleece Hoodies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20118·2020-05-07

    Poppin' Cobs Microwave Popcorn Recalled for Fire and Burn Hazards

    Fully Popped is recalling Poppin' Cobs 10 Pack Microwave Popcorn because the paper bags can catch fire in the microwave, posing fire and burn hazards.

    Product
    Poppin' Cobs 10 Pack Microwave Popcorn
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1806-2020·2020-05-06

    Philips TraumaDiagnost X-Ray System Recalled Due to Potential Shaft Failure

    Philips North America is recalling 346 TraumaDiagnost X-Ray systems because a shaft may break due to material fatigue, causing the arm to fall and potentially injure patients or staff.

    Product
    Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1747-2020·2020-05-06

    Vascular Solutions Recalls Langston Dual Lumen Catheters Due to Separation Risk

    Vascular Solutions is recalling Langston Dual Lumen Catheters because the inner lumen may separate from the hub during pressure injection.

    Product
    Langston Dual Lumen Catheter 6F Model 5540. For delivery of contrast medium in angiographic studies
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1257-2020·2020-05-06

    B. Braun Recalls Ceftazidime and Dextrose Injection Due to Stability Failures

    B. Braun Medical Inc. is recalling one lot of Ceftazidime for Injection USP and Dextrose for Injection USP because the product failed stability specifications for high molecular weight polymers.

    Product
    Ceftazidime for Injection USP and Dextrose for Injection USP, 2 g, 50 mL Duplex Container, RX only, B Braun Medical Inc., Bethlehem, PA 18018-3524, NDC 0264-3145-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1825-2020·2020-05-06

    Elekta MONACO RTP System Recalled for Potential Inaccurate Radiation Dose Delivery

    Elekta Inc is recalling 96 MONACO RTP systems because the software may alter contour shapes, potentially resulting in inaccurate radiation dose delivery to patients.

    Product
    Elekta MONACO RTP Sytem, radiation treatment planning software system - Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1814-2020·2020-05-06

    Welch Allyn X12+ Telemeter and Patient Cable Recall for Defibrillation Safety

    Welch Allyn is recalling X12+ Telemeters and patient cables because they may not meet defibrillation withstand requirements.

    Product
    X12+ and patient cable for the X12+ Telemeter with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL 10WIRE LEADFORM IEC SNAP, PAT CBL 10WIRE LEADFORM XL AHA SNAP, PAT CBL 10WIRE LEADFORM XL IEC SNAP, PAT CBL 4WIRE AHA SNAP HC.
    Category
    Medical Device
    Distribution
    Distributed nationwide