The Recall Desk

State

Nebraska product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34176–34200 of 78317

  • SevereNHTSA·19V700000·2019-10-03

    Jayco Eagle Recreational Trailers Recalled for Carbon Monoxide Risk

    Jayco is recalling 2019 Eagle HT and Eagle recreational trailers because the gas range does not vent outside, creating a carbon monoxide hazard.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E066000·2019-10-03

    GM Recalls Rugged Liner Tonneau Covers for Installation Defect

    General Motors is recalling Rugged Liner tri-fold soft tonneau covers for 2019-2020 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because difficult instructions may lead to incorrect installation.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V703000·2019-10-03

    Honda Recalls 2019 CRF450L Motorcycles Due to Horn Mount Defect

    Honda is recalling 2019 CRF450L motorcycles because the horn mount may break, allowing the horn to detach and interfere with handling or become a road hazard.

    Product
    HONDA — HONDA CRF450L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E065000·2019-10-03

    SynTec Recalls School Bus Seats for Insufficient Impact Absorption

    SynTec Seating Solutions is recalling S3B and S3C Base Convertible school bus seats because they may lack sufficient impact absorption, increasing injury risk in crashes.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V702000·2019-10-03

    Jayco Recalls 2017 Pinnacle Fifth Wheel Trailers Due to Suspension Defect

    Jayco is recalling 2017 Pinnacle Fifth Wheel trailers because the suspension may allow tires to contact the structure, causing damage and increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL PINNACLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V706000·2019-10-03

    Jayco Recalls 2016-2017 Alante Motorhomes Due to Fire Risk

    Jayco is recalling 2016-2017 Alante motorhomes because a missing heat shield may expose hydraulic lines to excessive heat, increasing the risk of a fire.

    Product
    JAYCO — JAYCO ALANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20004·2019-10-03

    VIQUA Recalls Solenoid Valve Kits for UV Water Treatment Systems

    VIQUA is recalling solenoid valve kits for UV water treatment systems because electrical current could leak, posing a shock hazard. No injuries have been reported.

    Product
    VIQUA Solenoid Valve Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0125-2020·2019-10-02

    FDA Recalls Quinacrine Dihydrochloride Bulk API Due to Labeling Error

    Darmerica, LLC is recalling 1.8 kilograms of bulk Quinacrine Dihydrochloride API because testing revealed the product was actually Artemisinin.

    Product
    Quinacrine Dihydrochloride (98.25%), bulk API product, packaged in a) 500 g NDC# 71052-530-05; b) 50 g NDC# 71052-530-55, c) 25g NDC# 71052-530-25, Darmerica LLC 198 Wilshire Blvd Casselberry, FL 32707
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1881-2019·2019-10-02

    Johnson Matthey Recalls Cisplatin Active Pharmaceutical Ingredient Due to Glass Contamination

    Johnson Matthey Inc. is recalling 26,625 grams of Cisplatin Active Pharmaceutical Ingredient due to potential glass contamination.

    Product
    Cisplatin Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V698000·2019-10-02

    BMW Recalls 2000-2002 Models for Driver Air Bag Inflator Defect

    BMW is recalling 2000-2002 323, 325, and 330 models because the driver-side air bag inflator may explode, posing a risk of serious injury or death.

    Product
    BMW — BMW 330, 325, 323
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V696000·2019-10-02

    Lamborghini Recalls 2017-2019 Aventador S Models Due to Engine Stall Risk

    Lamborghini is recalling 441 Aventador S vehicles because engine software may cause the engine to stall when coasting to a stop, increasing crash risk.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR S ROADSTER, AVENTADOR S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2552-2019·2019-10-02

    Sentinel CH SpA Recalls Alinity c Lithium Reagent Kits

    Sentinel CH SpA is recalling Alinity c Lithium Reagent Kits due to a potential carryover issue that may result in falsely elevated lithium patient results.

    Product
    Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 08P5320
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V697000·2019-10-02

    BMW Recalls 2020 S1000 RR Motorcycles Due to Oil Cooler Hose Defect

    BMW is recalling 416 2020 S1000 RR motorcycles because oil cooler hoses may not be attached properly, potentially causing an oil leak that increases crash risk.

    Product
    BMW — BMW S1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2561-2019·2019-10-02

    Elekta Monaco RTP System Recalled for Potential Dose Calculation Errors

    Elekta Inc is recalling 49 Monaco RTP Systems because unintentional changes to electron density settings may cause incorrect dose calculations for radiation therapy plans.

    Product
    Monaco RTP System, 5.50/5.51, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment plans…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2756-2019·2019-10-02

    Medline Electric Surgical Clipper Recalled for Overheating Charger Base

    Medline Industries is recalling 500 electric surgical clippers because a defective circuit board component may cause the charger base to overheat and malfunction.

    Product
    MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE, REF DYND70800 Product Usage: Medline Surgical Clipper is intended for the removal of body hair from the patient as required prior to surgery or other minor procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V695000·2019-10-02

    Daimler Recalls 2018-2019 Sprinter Vehicles for Inactive Airbag Systems

    Daimler Vans USA is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vans because their airbag systems may not have been activated, increasing crash injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 4500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V693000·2019-10-02

    Mercedes-Benz Recalls 2018-2019 Sprinter and Metris Vans for Safety Inspection

    Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Sprinter and Metris vans because they left the reassembly plant without final quality inspection of safety-relevant parts.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS, SPRINTER 3500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2560-2019·2019-10-02

    Elekta Monaco RTP System Recalled for Potential Dose Calculation Errors

    Elekta Inc is recalling 30 units of the Monaco RTP System 5.40 Unity because unintentional changes to electron density settings may result in incorrect dose calculations for radiation treatment plans.

    Product
    Monaco RTP System, 5.40 Unity, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2556-2019·2019-10-02

    Arrow Central Venous Catheterization Kit Recalled for Incorrect Banner Card

    Arrow International Inc is recalling 231 units of 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kits because they may contain the incorrect banner card.

    Product
    Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2551-2019·2019-10-02

    Sentinel CH SpA Recalls MULTIGENT Lithium Reagent Kits

    Sentinel CH SpA is recalling 15,919 MULTIGENT Lithium reagent kits due to a potential carryover issue that may cause falsely elevated patient results.

    Product
    MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 8L25-30
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1882-2019·2019-10-02

    FDA Recalls Oxaliplatin Active Pharmaceutical Ingredient Due to Glass Contamination

    Johnson Matthey Inc. is recalling Oxaliplatin Active Pharmaceutical Ingredient due to potential glass contamination. The product was distributed nationwide in the United States.

    Product
    Oxaliplatin Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001, NDC 49821-0075-XX
    Category
    Drug
    Distribution
    Distributed nationwide