The Recall Desk

State

Nebraska product recalls

73,106 recalls have nationwide distribution and so reach Nebraska. 4,575 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,575
Critical
715
Severe
1,131
Most recent
2026-09-23

Of the 4,575 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,131 (25%) are Severe.

These figures cover only the 4,575 recalls whose distribution notice names Nebraska specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12501–12525 of 77681

  • SevereNHTSA·24V238000·2024-03-28

    Chrysler minivan windshields may not be properly bonded to the vehicle

    Chrysler is recalling certain 2024 Pacifica and Voyager vehicles whose windshields may not have been properly bonded, allowing them to detach during a crash. This fails FMVSS 212.

    Product
    CHRYSLER — CHRYSLER VOYAGER, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V237000·2024-03-28

    Chevrolet Colorado and GMC Canyon front wheel hub bolts may break

    General Motors is recalling certain 2023 Chevrolet Colorado and GMC Canyon vehicles because front wheel hub bolts may have been over-tightened and damaged during installation.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24177·2024-03-28

    BJ's Wholesale Club Recalls Berkley Jensen 72-inch Tiki Torches for Burn Hazard

    BJ's Wholesale Club is recalling about 90,000 Berkley Jensen Citronella 72-inch Tiki Torches because the torch top can break open or fall off while lit, creating a burn hazard. The company has received nine reports of the top breaking or falling, including two burn injuries.

    Product
    Berkley Jensen Citronella 72-inch Tiki Torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24742·2024-03-28

    Forias Pack and Play Mattresses Recalled for Infant Suffocation Hazard

    Forias pack and play mattresses sold on Amazon.com from May through August 2023 violate federal crib mattress safety standards and pose a suffocation hazard to infants. The product is missing required warnings and labels.

    Product
    Forias Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V239000·2024-03-28

    Jeep Cherokee turn signals may not self-cancel after a turn

    Chrysler is recalling certain 2022 Jeep Cherokee vehicles because the turn signal self-cancelling feature may not work properly, failing FMVSS 108.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V241000·2024-03-28

    Micro Bird Recalls One 2019 G5 Transit Bus for Defrosting Defect

    Micro Bird is recalling one 2019 G5 Transit Bus because a module failure may disable the windshield defrosting system, reducing visibility.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V242000·2024-03-28

    Micro Bird Recalls 2019 G5 School Buses for Defrosting System Defect

    Micro Bird is recalling 2019 G5 school buses because a module failure may disable the windshield defrosting system, reducing driver visibility.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V240000·2024-03-28

    Chrysler minivan traction control does not work with cruise control active

    Chrysler is recalling certain 2024 Pacifica and Voyager vehicles because the traction control system does not function while cruise control is activated. A free software update is the remedy.

    Product
    CHRYSLER — CHRYSLER VOYAGER, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24741·2024-03-28

    Polaris Model Year 2022–2023 Snowmobiles Recalled for Fire Hazard

    Polaris is recalling about 7,000 Model Year 2022–2023 snowmobiles equipped with PATRIOT BOOST engines because the fuel line between the fuel rails can leak, posing a fire hazard. Consumers should stop using the recalled snowmobiles and contact Polaris for a free repair.

    Product
    Model Year 2022-2023 Snowmobiles equipped with PATRIOT BOOST Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24176·2024-03-28

    Purefog High Density Natural Fog Juice Liquid Recalled for Mold Risk

    Pure Brands of California is recalling Purefog High Density Natural Fog Juice Liquid because the product can expire sooner than the printed expiration date, posing a mold-exposure risk to people with compromised immune systems, damaged lungs, or mold allergies.

    Product
    Purefog High Density Natural Fog Juice Liquids
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1082-2024·2024-03-27

    Stonewall Kitchen Gluten Free Doughnut Mix Recalled for Undeclared Wheat

    Stonewall Kitchen is recalling Cinnamon Sugar Doughnut Mix (Gluten Free) with use-by dates of March 9-10, 2025, because units contain undeclared wheat. Consumers with wheat allergies or celiac disease should not consume this product.

    Product
    Stonewall Kitchen Cinnamon Sugar Doughnut Mix; Gluten Free; Home-Baked & Gluten Free; Net Wt. 18oz (510g); UPC: 1138131332
    Category
    Food
    Distribution
    44 states
  • SevereNHTSA·24V233000·2024-03-27

    2025 Peterbilt and Kenworth Trucks Recalled Over Steering Gear Defect

    PACCAR is recalling certain 2025 Peterbilt and Kenworth trucks because the steering gear sector shaft may have been improperly heat-treated, which can cause the gear teeth to crack or fracture.

    Product
    PETERBILT — PETERBILT, KENWORTH 579, T680, T280, T380
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1300-2024·2024-03-27

    FDA Recalls HeartMate II Left Ventricular Assist Systems for Graft Obstruction

    Thoratec Corp. recalls HeartMate II left ventricular assist system kits due to outflow graft deformation that could obstruct blood flow. The FDA has classified this as a Class I recall affecting 2,240 units distributed worldwide.

    Product
    HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate II LVAS Implant Kit, US REF 106015 3. HeartMate II LVAS Implant Kit, OUS REF 106016 Update (February 14, 2024) HeartMate II Left Ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V236000·2024-03-27

    Heartland RV Cooktop LED Backlight Circuit Fire Risk Recall

    Heartland is recalling 10,038 model year 2023-2024 fifth wheels and travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat, increasing the risk of a fire.

    Product
    HEARTLAND — HEARTLAND PROWLER, SOUTH FORK, SUNDANCE, MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0393-2024·2024-03-27

    FDA Recalls Unapproved Tianeptine Elixir Drug Product Nationwide

    Neptune's Fix Tianeptine Elixir, distributed nationwide by Super Chill Products, is recalled because it contains tianeptine, a substance not approved by the FDA for any medical use in the United States. Consumers should not use this product.

    Product
    Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1301-2024·2024-03-27

    HeartMate 3 Left Ventricular Assist System recalled for outflow graft obstruction

    The FDA is recalling the HeartMate 3 Left Ventricular Assist System due to observed outflow graft deformation that can obstruct blood flow. Patients with implanted devices should contact their healthcare provider.

    Product
    HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3 Sealed Outflow Graft with Bend Relief, US 3. HeartMate 3 Sealed Outflow Graft with Bend Relief, OUS 4. HeartMate 3…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V235000·2024-03-27

    Cruiser RV Recalls Travel Trailers Due to Cooktop Fire Risk

    Cruiser RV is recalling 2023-2024 travel trailers and fifth wheels because a faulty LED circuit board in the cooktop may overheat and cause a fire.

    Product
    CRUISER — CRUISER, CRUISER RV MPG, STRYKER, TWILIGHT, AVENIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1267-2024·2024-03-27

    ARROW QuickFlash Radial Artery Catheters Recalled for Defective Component

    ARROW International is recalling 1,160,470 QuickFlash radial artery catheterization devices due to a defective guidewire handle that can cause arterial vasospasm and vessel injury.

    Product
    ARROW QuickFlash Radial Artery Catherization (wire, guide, catheter), Part Numbers: a) REF AK-04220; b) REF ASK-04220-FMH1; c) REF ASK-04220-HHC; d) REF ASK-04220-KSP; e) REF ASK-04220-PSU; f) REF ASK-04220-UCL1; g) REF ASK-04500-AH; h) REF ASK-04500-HF-S; i)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V234000·2024-03-27

    Keystone RV Company Recalls Certain RV Models Due to Cooktop Fire Risk

    Keystone RV Company is recalling various 2021-2024 RV models because the cooktop LED backlight circuit board may overheat and increase the risk of fire.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN, CROSSROADS FUZION, MONTANA, ASPEN TRAIL, MONTANA HIGH COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1274-2024·2024-03-27

    Smiths Medical Pneupac paraPAC plus 310 ventilators recalled for malfunction

    Smiths Medical is recalling paraPAC plus 310 ventilators that may malfunction by delivering continuous gas flow instead of cycling breaths. The defect affects 10,140 units distributed worldwide and prevents proper ventilation.

    Product
    smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1275-2024·2024-03-27

    Smiths Medical Pneupac Plus 300 Ventilator Cycling Malfunction

    Smiths Medical Pneupac Plus 300 ventilators may intermittently deliver continuous airflow instead of cycling breaths as designed. This malfunction affects 2,902 units distributed worldwide.

    Product
    smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1320-2024·2024-03-27

    Medical Device Recall: Orthopedic Compression Screws with Incorrect Dimensions

    In2Bones, SAS is recalling I.B.S Compression screws due to a batch mix-up. Affected screws may have different lengths than indicated on their labels, creating a risk of improper surgical implantation.

    Product
    I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1342-2024·2024-03-27

    Surgical Guidewire Introducer Sheath Recalled for Internal Manufacturing Defects

    Angiodynamics vascular guidewire introducers (600 units) may have internal defects preventing proper function during surgery. Defects could cause procedure delays and require device exchange.

    Product
    MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-762
    Category
    Medical Device
    Distribution
    Distributed nationwide