The Recall Desk

State

Nebraska product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52401–52425 of 78404

  • SevereNHTSA·16V261000·2016-04-29

    Mercedes-Benz and Freightliner Sprinter Vans Recalled for Window Separation Risk

    Daimler Vans USA is recalling 2015-2016 Mercedes-Benz and Freightliner Sprinter vans because multiple paint layers may cause windows to separate in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V259000·2016-04-29

    Monroe Truck Equipment Recalls 2013 Ford F-550 Trucks with IMT Cranes

    Monroe Truck Equipment is recalling one 2013 Ford F-550 truck equipped with an IMT crane because the valve bank cover may crack and fall off, creating a road hazard.

    Product
    MONROE — MONROE FORD F-550 W/IMT CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V258000·2016-04-29

    Forest River Cardinal RVs Recalled for Incorrect Tire Placard Information

    Forest River is recalling 2016-2017 Cardinal RVs because the tire placard lists incorrect tire and rim specifications, which could lead to under-inflation and tire blowouts.

    Product
    FOREST RIVER — FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16C005000·2016-04-29

    Kiddy USA Recalls World Plus Child Seats Due to Buckle Defect

    Kiddy USA is recalling World Plus child seats because the harness buckle may not fully latch, increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS/CROTCH BUCKLE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V252000·2016-04-28

    Newmar Recalls 2014-2016 Motorhomes Due to Brake Signal Defect

    Newmar is recalling 1,150 recreational vehicles because the brake signal to towed devices may not deactivate, causing dragging brakes, overheating, or fire.

    Product
    NEWMAR — NEWMAR LONDON AIRE, ESSEX, MOUNTAIN AIRE, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V256000·2016-04-28

    GM Recalls 2016-2017 Trucks and SUVs for Front Control Arm Weld Defect

    General Motors is recalling specific 2016-2017 Chevrolet, GMC, and Cadillac vehicles because inadequate welds on the front upper control arms may separate, compromising steering and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO 1500, SIERRA 1500, TAHOE, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E039000·2016-04-28

    RAM ProMaster Trailer Light Module Recall for Brake Light Failure

    Chrysler is recalling RAM ProMaster Trailer Light Modules due to a software error that can prevent trailer brake lights from illuminating, increasing crash risk.

    Product
    RAM — RAM PROMASTER, PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V255000·2016-04-28

    Legacy Equipment Recalls Dominator Trucks Due to Crane Cover Defect

    Legacy Equipment is recalling 2013-2016 Dominator trucks because a crane valve bank cover may crack and fall off, creating a road hazard.

    Product
    LEGACY EQUIPMENT — LEGACY EQUIPMENT DOMINATOR II, DOMINATOR III, DOMINATOR IV, DOMINATOR-PROPANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V254000·2016-04-28

    Custom Truck Recalls Dominator Trucks with IMT Crane Valve Cover Defect

    Custom Truck is recalling 2013-2016 Dominator trucks equipped with specific IMT cranes because the valve bank cover may crack and fall off, creating a road hazard.

    Product
    CUSTOM TRUCK — CUSTOM TRUCK DOMINATOR I, DOMINATOR-PROPANE, DOMINATOR IV, DOMINATOR III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V253000·2016-04-28

    RAM ProMaster Recall for Trailer Brake Light Software Error

    Chrysler is recalling 2014-2016 RAM ProMaster and 2015-2016 ProMaster City vehicles because a software error may prevent trailer brake lights from illuminating, increasing crash risk.

    Product
    RAM — RAM PROMASTER, PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·16V257000·2016-04-28

    GM Recalls 2013-2016 Chevrolet Vehicles for Theft Protection Software Defect

    General Motors is recalling certain 2013-2016 Chevrolet Sonic, Trax, and Spark vehicles because the radio software may fail to provide an audible warning chime, increasing the risk of vehicle theft.

    Product
    CHEVROLET — CHEVROLET TRAX, SPARK, SONIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1529-2016·2016-04-27

    Mevion S250 Proton Therapy System Recalled for Gantry Motion Hazard

    Mevion Medical Systems is recalling five MEVION S250 proton therapy systems because an aperture may fall out during gantry motion, posing a risk of traumatic injury or death to patients.

    Product
    MEVION S250 for Proton Radiation Therapy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0825-2016·2016-04-27

    Impax Recalls Dextroamphetamine Sulfate Tablets Due to Failed Impurity Specifications

    Impax Laboratories is recalling 67,428 bottles of Dextroamphetamine Sulfate Tablets USP, 10 mg, because the product failed impurities and degradation specifications.

    Product
    Dextroamphetamine Sulfate Tablets USP, 10 mg, 100-count bottle, Rx only, Manufactured and Distributed by: Corepharma, LLC, Middlesex, NJ 08846, NDC 64720-0216-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V248000·2016-04-27

    Ford Recalls 2011-2012 F-150, Mustang, Expedition, Navigator for Transmission Defect

    Ford is recalling specific 2011-2012 F-150, Mustang, Expedition, and Navigator vehicles because the automatic transmission may unexpectedly downshift to first gear, increasing crash risk.

    Product
    FORD — FORD, LINCOLN F-150, MUSTANG, EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1342-2016·2016-04-27

    Boston Scientific Recalls Fetch 2 Aspiration Catheters Due to Shaft Breaks

    Boston Scientific is recalling Fetch 2 Aspiration Catheters because the catheter shafts may break, potentially requiring additional procedures to remove the broken piece from patients.

    Product
    Boston Scientific Fetch 2 Aspiration Catheter, Catalog No. 109400-001. Product The Fetch 2 Aspiration Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the peripheral and coronary vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V249000·2016-04-27

    2016 Jeep Grand Cherokee Recall for Brake Shift Interlock Defect

    Chrysler is recalling 2016 Jeep Grand Cherokee vehicles because a loose electrical connection in the brake transmission shift interlock solenoid may cause the transmission to lock in Park or Neutral.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0832-2016·2016-04-27

    Hospira Recalls Potassium Chloride Injection Bags Due to Chemical Contamination

    Hospira Inc. is recalling 81,888 bags of Potassium Chloride Injection due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7077-14
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1530-2016·2016-04-27

    Acorn 180 Curved Stairlift Recalled Due to Broken Rivets

    Acorn Stairlifts Inc is recalling 1,290 Acorn 180 Curved Stairlifts in the US because aluminum rivets may break under prolonged use.

    Product
    Acorn 180 Curved Stairlift
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0828-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination

    Hospira Inc. is recalling 4,368 bags of Dextrose Injection, USP, 50% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 50%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7936-19, Barcode (01) 0 030409 793619 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0829-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination Risk

    Hospira Inc. is recalling 552 bags of Dextrose Injection, USP, 20% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7935-19, Barcode (01) 0 030409 793519 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0826-2016·2016-04-27

    Impax Recalls Dextroamphetamine Sulfate Tablets Due to Failed Impurity Specifications

    Impax Laboratories is recalling specific lots of Dextroamphetamine Sulfate Tablets because they failed impurity and degradation specifications.

    Product
    Dextroamphetamine Sulfate Tablets USP, 5 mg, 100-count bottle, Rx only, Manufactured and Distributed by: CorePharma, LLC, Middlesex, NJ 08846, NDC 64720-215-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1515-2016·2016-04-27

    Ossur Lil Angel Vest Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling Lil Angel Vest P3 Sorbatex units because the plastic stabilizer strap may partially or completely fracture.

    Product
    Ossur Lil Angel Vest P3 Sorbatex. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide