The Recall Desk

State

Nebraska product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37501–37525 of 78321

  • SevereNHTSA·19V179000·2019-03-06

    Porsche Recalls 2018 Models for Loose Side Air Bag Sensors

    Porsche is recalling 417 vehicles because side air bag impact sensors may not be properly tightened, which could prevent air bag deployment in a crash.

    Product
    PORSCHE — PORSCHE 911, 718 BOXSTER, 718 CAYMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V181000·2019-03-06

    Karma Recalls 2012 Fisker Karma Vehicles for Air Bag Inflator Defect

    Karma Automotive is recalling 2012 Fisker Karma vehicles because passenger frontal air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    FISKER — FISKER KARMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V172000·2019-03-06

    Jayco Recalls 2018 Fifth Wheel Trailers Due to Fuel Tank Hardware Issue

    Jayco is recalling 2018 Talon and Seismic fifth wheel trailers because incorrect hardware may fail to secure the auxiliary fuel tank, increasing the risk of a fire.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL TALON, SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0888-2019·2019-03-06

    Philips MRI System Recall Due to Ceiling Speaker Magnetic Hazard

    Philips is recalling Intera Achieva 1.5T Nova MRI systems because ceiling speakers may be pulled by the magnetic field and fall.

    Product
    Intera Achieva 1.5T Nova, Model Number 781172. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0927-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T for PET, Model Number 781477. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0923-2019·2019-03-06

    Philips Ingenia Elition X MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia Elition X MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia Elition X, Model Number 781358. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0893-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T, Model Number 781177. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0926-2019·2019-03-06

    Philips MR RT MRI Systems Recalled for Falling Ceiling Speaker Hazard

    Philips is recalling MR RT MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    MR RT, Model Number 781439. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V188000·2019-03-06

    Volkswagen Recalls 56,173 Vehicles for Rear Coil Spring Fracture Risk

    Volkswagen is recalling 56,173 vehicles because rear coil springs may fracture prematurely, potentially causing tire damage and loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF, JETTA, GOLF SPORTWAGEN, TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V178000·2019-03-06

    Entegra Recalls 2019-2020 Reatta Motorhomes for Damaged Tow Hitch

    Entegra Coach is recalling 2019-2020 Reatta motorhomes because the tow hitch may have been damaged during delivery, increasing the risk of a crash.

    Product
    ENTEGRA — ENTEGRA REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0895-2019·2019-03-06

    Philips Intera 1.5T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.5T, Model Number 781195. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0873-2019·2019-03-06

    Philips Multiva MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling 11,226 Multiva MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0876-2019·2019-03-06

    Philips Intera 1.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Power/Pulsar, Model Number 781103. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V177000·2019-03-06

    Jayco Recalls 2019-2020 Embark Motorhomes Due to Hitch Damage

    Jayco is recalling 2019-2020 Embark motorhomes because the hitch may have been damaged during delivery, increasing the risk of a crash if the towed vehicle separates.

    Product
    JAYCO — JAYCO EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0915-2019·2019-03-06

    Philips Achieva 1.5T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 1.5T Conversion, Model Number 781346. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0901-2019·2019-03-06

    Philips Ingenia MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling Ingenia 1.5T CX MRI systems because ceiling speakers may be pulled by the magnetic field and fall.

    Product
    Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0918-2019·2019-03-06

    Philips Ingenia 3.0T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0916-2019·2019-03-06

    Philips Ingenia 1.5T S MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 1.5T S MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0885-2019·2019-03-06

    Philips Intera IT MRI Systems Recalled for Falling Ceiling Speaker Risk

    Philips is recalling 11,226 Intera IT MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera IT, Model Number 781160. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0904-2019·2019-03-06

    Philips Ingenia 3.0T CX MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 3.0T CX MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 3.0T CX, Model Number 781271. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0897-2019·2019-03-06

    Philips Achieva 7.0T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 7.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 7.0T, Model Number 781240. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0875-2019·2019-03-06

    Philips MRI Systems Recalled Due to Ceiling Speaker Fall Risk

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0948-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that could cause leaks and reduced drug delivery.

    Product
    AF 550 x 5ML/HR 2ML 60LO CPNB, Product code MT5060XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V168000·2019-03-06

    Highland Ridge RV Recalls 2019 Travel Trailers Due to Incorrect Weight Label

    Highland Ridge RV is recalling 74 units of 2019 Mesa Ridge and Open Range Ultra Lite travel trailers because the weight label exceeds the safety chain rating.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE ULTRA LITE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide