The Recall Desk

State

Nebraska product recalls

73,566 recalls have nationwide distribution and so reach Nebraska. 4,576 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,576
Critical
715
Severe
1,343
Most recent
2026-10-14

Of the 4,576 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 1,343 (29%) are Severe.

These figures cover only the 4,576 recalls whose distribution notice names Nebraska specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25551–25575 of 78142

  • HighNHTSA·21V619000·2021-08-06

    Hyundai Recalls Sonata, Accent, Azera, and Sonata Hybrid for Trunk Latch Defect

    Hyundai is recalling specific 2016-2020 Sonata, Sonata Hybrid, Accent, and Azera vehicles because a damaged trunk latch may prevent opening from the inside, risking entrapment.

    Product
    HYUNDAI — HYUNDAI SONATA, SONATA HYBRID, AZERA, ACCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V616000·2021-08-06

    2021 Volkswagen Atlas Relays Pose Fire Risk, Recall Issued

    Volkswagen is recalling 2021 Atlas and Atlas Cross Sport vehicles with damaged relays that may activate the horn or starter indefinitely, creating a fire hazard. Dealers will replace affected relays free of charge.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V615000·2021-08-06

    2022 Volkswagen Taos Engine Stall Software Defect Recall

    Volkswagen recalls 2022 Taos all-wheel-drive vehicles for a software defect that may cause engine stall when stopping, increasing crash risk. Dealers will update the engine control unit software free of charge.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V610000·2021-08-05

    Tiffin Wayfarer motorhomes 2017-2022 hitch extension failure and detachment risk

    Tiffin is recalling 2017-2022 Wayfarer motorhomes because the hitch extension may fail under stress, causing the hitch to detach and increasing crash risk. Dealers will inspect and replace the hitch and reinforce the frame rail extension at no charge.

    Product
    TIFFIN — TIFFIN WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V613000·2021-08-05

    2021 Maserati Tire Placard Recall: Incorrect Pressure Information

    Maserati is recalling certain 2021 Ghibli and Quattroporte vehicles with 21-inch tires due to incorrect tire pressure information on the placard. Improper tire inflation could affect vehicle stability and control.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V612000·2021-08-05

    2022 Chevrolet Equinox and Terrain tire recall for tread separation risk

    General Motors is recalling 2021-2022 Chevrolet Equinox and GMC Terrain vehicles with certain Hankook tires that may have insufficient curative agent, risking tread separation and loss of vehicle control.

    Product
    CHEVROLET — CHEVROLET, GMC EQUINOX, TERRAIN, TERRAIN NA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V611000·2021-08-05

    Cadillac CT4 and CT5 roof rail air bags installation defect

    General Motors is recalling 2020-2022 Cadillac CT4 and CT5 vehicles because roof rail side-curtain air bags may not have been installed correctly. Improper installation could prevent proper deployment during a crash.

    Product
    CADILLAC — CADILLAC CT4, CT5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V606000·2021-08-05

    2021 Audi RS Q8 rear seat belt retractors may deactivate prematurely

    Certain 2021 Audi RS Q8 vehicles have rear seat belt retractors that may deactivate prematurely, preventing child restraint systems from securing properly. Dealers will repair affected components free of charge.

    Product
    AUDI — AUDI, VOLKSWAGEN S5 CABRIOLET, S8, A6, Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21176·2021-08-04

    Sling Loungers Recalled for Amputation, Laceration, and Pinching Hazard

    About 155,000 True Living Sling Loungers sold at Dollar General are recalled because the frames can collapse unexpectedly, causing amputation and laceration injuries when fingers get caught in metal folding joints. Three amputations or lacerations have been reported.

    Product
    True Living Sling Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2158-2021·2021-08-04

    Zippie Voyage Early Intervention Stroller Seating System Detachment

    Sunrise Medical is recalling the Zippie Voyage early intervention stroller due to unexpected seating system detachment that can cause falls and injury. Approximately 4,741 devices are affected worldwide.

    Product
    Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of assisting a disabled person while providing supportive elements for assisted transportation and seating for a child or small adult not to exceed 75 pounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0800-2021·2021-08-04

    Randall Mixed Beans Recall Due to Temperature Control Failure

    Randall Foods, Inc. is recalling Randall Mixed Beans in 48oz, 24oz, and 15.4oz glass jars due to lack of functioning temperature indicating devices in retorts used during processing. The affected products were distributed to retail locations in 22 states.

    Product
    RANDALL MIXED BEANS 48OZ glass jars UPC 070095000407; RANDALL MIXED BEANS 24OZ glass jars UPC 070095000414; RANDALL MIXED BEANS 15.4OZ glass UPC 070095000430
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-2157-2021·2021-08-04

    Zippie Voyage Early Intervention Stroller Seating System May Detach

    Sunrise Medical recalls Zippie Voyage early intervention strollers because the seating system may unexpectedly detach and fall, causing injury. Approximately 9,865 devices are affected.

    Product
    Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of assisting a disabled person while providing supportive elements for assisted transportation and seating for a child or small adult not to exceed 75 pounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0803-2021·2021-08-04

    Randall Black Beans Recall: Non-Functioning Temperature Devices

    Randall Foods, Inc. is recalling Randall Black Beans in 48 oz, 24 oz, and 15.4 oz glass jars due to non-functioning temperature indicating devices in retorts used during production, which may affect product safety.

    Product
    RANDALL BLACK BEANS 48OZ glass jars UPC 070095000605; RANDALL BLACK BEANS 24OZ glass jars UPC 070095000612; RANDALL BLACK BEANS 15.4OZ glass jars UPC 070095000636
    Category
    Food
    Distribution
    22 states
  • SevereCPSC·21175·2021-08-04

    LG Energy Solution Recalls RESU10H Home Batteries for Fire Hazard

    LG Energy Solution Michigan is recalling about 10,000 RESU10H lithium-ion residential energy storage batteries because they can overheat and catch fire, emitting harmful smoke. The firm has received five reports of batteries smoking and catching fire, resulting in property damage and one injury.

    Product
    LG Chem "RESU10H" Lithium-Ion Residential Energy Storage System Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2021·2021-08-04

    Eat Gangster Oatmeal Cookie Mix Recalled for Salmonella Contamination

    Eat Gangster Oatmeal Schmoatmeal Cookie Mix has been recalled due to potential Salmonella contamination in tigernut flour, an ingredient used in the product. The affected 8.5 oz bags were distributed nationwide.

    Product
    Eat GANGSTER, Oatmeal Schmoatmeal Cookie Mix, 8.5 Oz, Eat GANGSTER LLC, Wichita, KS, UPC 0 51497 13952 0
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0802-2021·2021-08-04

    Randall Navy Beans recalled due to non-functioning temperature devices

    Randall Foods is recalling Randall Navy Beans in 48 oz and 15.4 oz glass jars due to lack of functioning temperature indicating devices in retorts during processing.

    Product
    RANDALL NAVY BEANS 48OZ glass jars UPC 070095000506; RANDALL NAVY BEANS 15.4OZ glass jars UPC 070095000537
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Food)·F-0798-2021·2021-08-04

    Randall and Hurst's Great Northern Beans Recalled for Temperature Device Failure

    Randall Foods, Inc. is recalling Randall and Hurst's brand Great Northern Beans due to non-functioning temperature indicating devices in the canning equipment, which could allow underprocessed product to reach consumers.

    Product
    RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100; RANDALL GREAT NORTHERN BEANS 24OZ glass jar UPC 070095000117; RANDALL GREAT NORTHERN BEANS 15.4OZ glass jar UPC 070095000131; RANDALL ORGANIC GREAT NORTHERN BEANS 48OZ glass jar UPC 070095005105; Hurst's Fully Cooked…
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-2005-2021·2021-08-04

    Recirculator 8.0s Disposable Lavage Kit recalled for potential aluminum ion release

    Eight Medical International BV is recalling the Recirculator 8.0s Disposable Lavage Kit due to potential aluminum ion release during warming therapy that may expose patients under certain use conditions.

    Product
    Recirculator 8.0s Disposable Lavage Kit (product code number 8100) , GTIN: 08719992086016. Hyperthermic Perfusion System intended to raise the temperature of the thoracic or peritoneal cavity to a target temperature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0805-2021·2021-08-04

    Randall Ultimate 4-Bean Mix Recalled for Lack of Temperature Indicators

    Randall Foods, Inc. is recalling Randall Ultimate 4-Bean Mix in 48 oz glass jars due to non-functioning temperature indicating devices in retorts used during processing, which may affect proper sterilization.

    Product
    RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Food)·F-0799-2021·2021-08-04

    Randall Pinto Beans Recall Due to Temperature Control Defect

    Randall Foods, Inc. is recalling Randall Pinto Beans in three sizes (48oz, 24oz, and 15.4oz glass jars) distributed across 22 states due to lack of functioning temperature-indicating devices in retorts used during processing.

    Product
    RANDALL PINTO BEANS 48OZ glass jars UPC 070095000209; RANDALL PINTO BEANS 24OZ glass jars UPC 070095000216; RANDALL PINTO BEANS 15.4OZ glass jars UPC 070095000230
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Food)·F-0801-2021·2021-08-04

    Randall Kidney Beans Recall for Faulty Temperature Devices

    Randall Foods, Inc. is recalling Randall Kidney Beans in three sizes due to non-functioning temperature indicating devices in retorts, which may affect proper heat sterilization during processing.

    Product
    RANDALL KIDNEY BEANS 48OZ glass jars UPC 070095000308; RANDALL KIDNEY BEANS 24OZ glass jars UPC 070095000315; RANDALL KIDNEY BEANS 15.4OZ glass jars UPC 070095000339
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-2161-2021·2021-08-04

    OEC Elite Mobile C-Arm Recalled for Battery Depletion

    GE OEC Medical Systems is recalling 3,570 OEC Elite mobile C-arm imaging systems worldwide due to potential early depletion of the battery that monitors X-ray tube temperature, which could render the system inoperable.

    Product
    OEC Elite mobile C-arm - Product Usage: intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2151-2021·2021-08-04

    CooperVision Contact Lenses Recalled for Misaligned Axis Mark

    CooperVision is recalling MEDIFLEX ELITE 1 DAY TORIC daily disposable contact lenses (lot W0106167) due to misaligned axis marks that can cause blurred vision.

    Product
    MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide