The Recall Desk

State

Nebraska product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36626–36650 of 78318

  • SevereNHTSA·19E030000·2019-04-18

    Bendix Recalls Air Disc Brake Calipers for School Buses

    Bendix is recalling ADB22X Air Disc Brake Calipers for school buses because the driver side rear brakes may drag, increasing the risk of fire.

    Product
    SERVICE BRAKES, AIR:DISC recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19107·2019-04-18

    Tekno Recalls Tuff Smoke-Less Grills Due to Fire and Burn Hazards

    Tekno Products is recalling Tuff smoke-less grills because they can overheat, posing fire and burn hazards. Consumers should stop using the grills and return them for a refund.

    Product
    Tuff smoke-less grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V312000·2019-04-18

    GM Recalls 2017-2019 Chevrolet Trax for Front Suspension Weld Defect

    General Motors is recalling 2017-2019 Chevrolet Trax vehicles because improperly welded front lower-control arm joints may break, causing partial separation and increased crash risk.

    Product
    CHEVROLET — CHEVROLET TRAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V309000·2019-04-18

    2019 Mercedes-Benz Sprinter Recalled for High-Beam Software Error

    Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vans because a software error may prevent drivers from turning off high beams, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V316000·2019-04-18

    Nissan Recalls 2019 Altima Vehicles Due to Fuel Pump Lock Ring Defect

    Nissan is recalling 2019 Altima vehicles with front-wheel drive and 2.5-liter engines because a fuel pump lock ring may not be fully engaged, potentially causing a fuel leak and fire risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19108·2019-04-18

    Target Recalls Wooden Toy Vehicles Due to Choking Hazard

    Target is recalling Bullseye's Playground wooden toy vehicles because wheels can detach, posing a choking hazard to children.

    Product
    Bullseye's Playground wooden toy vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19739·2019-04-18

    RH Recalls Callum Canopy Beds Due to Falling Rail Injury Hazard

    RH is recalling Callum Canopy Beds because horizontal canopy rails can detach and fall. No injuries have been reported, but consumers should stop using the beds until repaired.

    Product
    Callum Canopy Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V313000·2019-04-18

    MobilityTrans Recalls Modified Ford and Ram Vans with Defective Foldaway Seats

    Mobility Transportation Services is recalling modified Ford and Ram vans because foldaway seats may not stay locked during a crash, increasing injury risk.

    Product
    FORD — FORD, RAM, MOBILITY SPECIALISTS TRANSIT, E-450, E-350, E-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1135-2019·2019-04-17

    FDA Recalls Leopard Miracle Honey Containing Undeclared Sildenafil

    USA LESS Inc. is recalling Leopard Miracle Honey because it contains undeclared sildenafil, an unapproved drug for erectile dysfunction.

    Product
    LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1 Sachet 15 gr / 0.53 Oz is labeled as LEOPARD Miracle of Honey, UPC 8 699415 912859, Manufactured in Turkey, www leopardhoneytr.com.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1300-2019·2019-04-17

    Theo Chocolate Sea Salt 70% Dark Chocolate Bars Recalled for Undeclared Milk

    Theo Chocolate is recalling Sea Salt 70% Dark Chocolate bars due to undeclared milk. The product was distributed nationwide.

    Product
    Sea Salt 70% Dark Chocolate 3 oz. bars, wrapped in foil and paper wrapper, brand Theo Chocolate, UPC 8 74492 00325 8. The Sea Salt 70% Dark Chocolate 3 oz. bar's label is read in part: "***Sea Salt 70% Dark Chocolate *** Ingredients: Cocoa Beans, Cane Sugar, Sea Salt, Ground…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1118-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA testing found an impurity above acceptable levels.

    Product
    Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/12.5mg, a) 30-count (NDC: 13668-117-30), b) 90-count (NDC: 13668-117-90) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1117-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium / Hydrochlorothiazide Tablets, USP 50mg/12.5mg, a) 30-count (NDC: 13668-116-30), b) 90-count (NDC: 13668-116-90), c) 1000-count (NDC: 13668-116-10) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1119-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/25mg, a) 30-count (NDC: 13668-118-30), b) 90-count (NDC: 13668-118-90), c) 1000-count (NDC: 13668-118-10) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1111-2019·2019-04-17

    McDaniel Life-Line Recalls Indian Herb Paste Due to Unapproved New Drug Status

    McDaniel Life-Line LLC is voluntarily recalling 150 vials of Indian Herb Paste because the product is an unapproved new drug. The recall covers distribution in the US, Italy, Australia, Canada, and Poland.

    Product
    Indian Herb Paste (a dietary supplement) Ingredients: Galangal, Indian Paint, Yellow Dock & Licorice in an alloy of Life-Line tm and Zinc Chloride in 6 dram vials, McDaniel Life-Line LLC, Dimmitt, TX
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1114-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 25 mg, because FDA labs found an impurity above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 25 mg, a) 90-count (NDC: 13668-113-90), b) 1000-count (NDC: 13668-113-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V311000·2019-04-17

    Hyundai Recalls 2019 Veloster Vehicles Due to Door Latch Defect

    Hyundai is recalling 12,438 2019 Veloster vehicles because the driver's door latch can fail in a side impact crash, potentially allowing the door to open.

    Product
    HYUNDAI — HYUNDAI VELOSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1116-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 100 mg, because FDA testing found an impurity above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 90-count (NDC: 13668-115-90), b) 1000-count (NDC: 13668-115-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1115-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 50 mg, because FDA testing found an impurity above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count (NDC: 13668-409-30), b) 90-count (NDC: 13668-409-90), c) 1000-count (NDC: 13668-409-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V304000·2019-04-17

    Spartan Recalls 2019 Utilimaster Truck Bodies Due to Electrical Fire Risk

    Spartan Motors is recalling 2019 Utilimaster Truck Bodies because undersized wires may overheat, melt, and cause an unexpected engine shutdown, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER TRUCK BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V308000·2019-04-17

    Volvo Recalls 2016 XC90 Vehicles for Coolant Hose Fire Risk

    Volvo is recalling 2016 XC90 vehicles because a coolant hose may crack and leak, potentially causing a fire in the catalytic converter area.

    Product
    VOLVO — VOLVO XC90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1100-2019·2019-04-17

    Edwards IntraClude Intra-Aortic Occlusion Device Recalled for Inter-Lumen Leak

    Edwards Lifesciences is recalling IntraClude Intra-Aortic Occlusion Devices due to a reported leak between the cardioplegia and pressure lumens.

    Product
    Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a 10.5 Fr (3.5mm), triple lumen, 100cm long catheter with an elastomeric balloon near its distal tip designed to occlude the ascending aorta in order to partition the aortic root from arterial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1276-2019·2019-04-17

    Trader Joe's Natural Creamer Recalled for Undeclared Milk Allergen

    Good Karma Foods is recalling Trader Joe's Natural Creamer - Vanilla because the product contains milk but the label does not list it as an ingredient.

    Product
    PL Trader Joe Natural Creamer - Vanilla 12/32oz, Plastic bottle, Distributed by Good Karma Foods, Inc. with manufacturing at Shamrock Foods at Phoenix, AZ., Keep refrigerated
    Category
    Food
    Distribution
    Distributed nationwide