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.

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.

31326–31350 of 78302

  • HighNHTSA·20V211000·2020-04-10

    Freightliner and Western Star trucks recalled for incorrect weight rating labels

    Daimler Trucks North America is recalling 2020-2021 Freightliner and Western Star commercial trucks with incorrect weight-rating labels. Incorrectly labeled trucks could be overloaded, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CORONADO, 114SD, 4700, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V213000·2020-04-09

    Hyundai Recalls 2020 Nexo and Sonata for Parking Software Defect

    Hyundai is recalling 2020 Nexo and Sonata vehicles because a software defect in the Remote Smart Parking Assist system may allow unintended vehicle movement, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI NEXO, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V209000·2020-04-09

    Forest River Recalls 2021 Starcraft Bus All Star Over Wiring Chafing

    Forest River is recalling 2021 Starcraft Bus All Star transit buses because a wire harness may chafe against the frame, potentially causing engine stalls or loss of braking stability.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V210000·2020-04-09

    StarCraft Starquest School Bus Recall for Wire Harness Chaffing

    Forest River is recalling 2022 StarCraft Starquest school buses because a wire harness may chafe against the frame, potentially causing engine stalls or loss of braking stability.

    Product
    STARCRAFT BUS — STARCRAFT BUS STARQUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V207000·2020-04-09

    RAM 2500 and 3500 Trucks Recalled for Bed Step Failure Risk

    Chrysler is recalling 2019-2020 RAM 2500 and 3500 trucks because the accessory bed step may fail during use, increasing injury risk.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E020000·2020-04-09

    Chrysler Recalls Mopar Rear Bed Step Kits for Ram Trucks

    Chrysler is recalling Mopar Rear Bed Step Kits for Ram heavy-duty trucks because the bed step may fail during side loading, increasing injury risk.

    Product
    STRUCTURE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V208000·2020-04-09

    Chrysler Recalls 2019-2020 Ram 1500 and Jeep Compass for Wiper Defect

    Chrysler is recalling 2019-2020 Ram 1500 and Jeep Compass vehicles because windshield wiper arms may loosen, reducing visibility and increasing crash risk.

    Product
    RAM — RAM, JEEP 1500, COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V202000·2020-04-08

    Great Dane Recalls 2020-2021 Everest Vans Due to Axle Nut Clip Defect

    Great Dane is recalling 2020-2021 Everest Refrigerated Vans because improperly installed axle nut retaining clips may cause loose wheels and loss of vehicle control.

    Product
    GREAT DANE — GREAT DANE EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V203000·2020-04-08

    Spartan Gladiator and MetroStar Recalled for Park Brake Line Defect

    Marion Body Works is recalling 2019-2020 Spartan Gladiator and MetroStar vehicles because the park brake control line may loosen, potentially causing sudden deceleration and increasing crash risk.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V206000·2020-04-08

    Vac-Tron Vacuum Excavator Trailers Recalled for Rear Impact Protection Defect

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because they may lack extended lower chassis, reducing rear impact protection and increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MINICOMBO, MC 873 SDT, MC 835 SDT, MC 833 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E019000·2020-04-08

    Agility Fuel Solutions Recalls CNG Pressure Relief Devices for Rupture Risk

    Agility Fuel Solutions is recalling certain CNG pressure relief devices that may fail to vent when exposed to heat, potentially causing the fuel system to rupture.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:PRESSURE RELIEF DEVICES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0871-2020·2020-04-08

    ReStructure Vanilla Protein Powder Recalled for Missing Milk Labeling

    New Capstone, Inc. is recalling ReStructure Vanilla Protein Powder because the ingredient statement does not include the word milk.

    Product
    ReStructure VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G SINGLE PACKET Other Ingredients: Non-GMO rBGH-Free Whey Protein Concentrate, Rice Bran and Germ*** Manufactured for & distributed by: New Capstone, Inc. 125 Trade Court, Suite F44, Mooresville, NC 28117 1-888-577-3703…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1622-2020·2020-04-08

    Philips V60 Ventilators Recalled for Power Management Board Failure

    Respironics is recalling 23,581 Philips V60 Ventilators because a solder connection failure on the power board may cause the blower to lose power or shut down unexpectedly, potentially leading to hypercarbia or hypoxemia.

    Product
    Philips V60 Ventilators with Power Management PCBA part number 1055906
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Devices)·Z-1567-2020·2020-04-08

    LeMaitre Embolectomy Catheter Recall for Deflation Failure and Tip Separation

    LeMaitre Vascular is recalling 5F Plus Over the Wire Embolectomy Catheters due to reports of deflation failure that may lead to tip separation.

    Product
    LeMaitre 5F Plus Over the Wire Embolectomy Catheter, Model Nos. 1651-84, e1651-84, 1651-88, e1651-88. The LeMaitre Over the Wire Embolectomy Catheter is indicated for use in the removal of emboli and thrombi during embolectomy and/or thrombectomy. It can also be used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·20107·2020-04-08

    Continuum Recalls Lenox Tea Kettles Due to Burn Hazard

    Continuum is recalling Lenox 2.5 Quart Tea Kettles because they can expel hot water, posing a burn hazard. Consumers should stop using the kettles and contact the company for a refund.

    Product
    Lenox 2.5 Quart Tea Kettles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1632-2020·2020-04-08

    Merits E604 Pilot Navigator Stairlift Recalled Due to Pinion Gear Defect

    Merits Health Products is recalling 82 E604 Pilot Navigator Stairlifts because the pinion gear may disengage from the track, allowing the lift to slip or jolt.

    Product
    Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1602-2020·2020-04-08

    Stryker Recalls Ceiling Mounted Surgical Light Systems Due to Fall Risk

    Stryker is recalling 1,415 Berchtold Chromophare Ceiling Mounted Surgical Light Systems because a missing snap ring or spanner nut may cause the light to fall.

    Product
    Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1633-2020·2020-04-08

    Physio-Control Recalls LifePAK 500 AEDs Due to Contact Plating Wear

    Physio-Control is recalling 173,459 LifePAK 500 AEDs because mechanical wear on the therapy connector may prevent the device from detecting a patient, potentially delaying treatment.

    Product
    LifePAK 500 Automated External Defibrillator, model numbers: 3005400-XXX, U3005400-XXX, 3011790-XXX/, U3011790-XXX - Product Usage: The LIFEPAK 500 AED is a semi-automatic defibrillator that uses a patented Shock Advisory System. This software algorithm analyzes the patient s…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0877-2020·2020-04-08

    Vitamin Cottage Almond Clusters Recalled for Undeclared Peanut and Milk Allergens

    Vitamin Cottage is recalling Natural Grocers Almond Clusters in Dark Chocolate because the product contains undeclared peanut and milk allergens.

    Product
    NATURAL GROCERS ALMOND CLUSTERS DK CHOCOLATE NON-GMO, 8 oz. (227g), packed in a plastic bag, UPC 000087236088, Packaged by Vitamin Cottage Natural Food Markets, Inc., Lakewood, CO 80228
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-1634-2020·2020-04-08

    Smith & Nephew Recalls NAVIO Soft Tissue Protector Due to Binding Risk

    Smith & Nephew is recalling 348 NAVIO Soft Tissue Protectors because the instrument may become stuck to bone pins during surgery.

    Product
    NAVIO Soft Tissue Protector, included in instrument kits. The NAVIO Tissue Protector is a reusable instrument designed to, when used as instructed, provide the required bone pin spacing for the Navio bone clamps and potentially reduce the amount of patient tissue affected…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1618-2020·2020-04-08

    Karl Storz C-MAC Video Laryngoscope Recall Due to Loose Glass Cover

    Karl Storz is recalling 27,165 C-MAC Video Laryngoscopes because the glass cover at the distal end may become loose during use or reprocessing, potentially delaying procedures or requiring removal from the body.

    Product
    Karl Storz SE & Co. KG, C-MAC Video Laryngoscope MIL # 1, for the following REF numbers: 1. 8403xx series, which includes: 8403AX, AXC, BX, BXC, DXC, EXC, GXC, HX, HXK, HXP, KXC, MXC 2. 8401xx series, which includes: 8401AX, AXC, BX, BXC, DXC, GXC, HX, HXP, KXC.…
    Category
    Medical Device
    Distribution
    Distributed nationwide