The Recall Desk

State

Nebraska product recalls

73,381 recalls have nationwide distribution and so reach Nebraska. 4,575 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,575
Critical
715
Severe
1,343
Most recent
2026-09-23

Of the 4,575 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 4,575 recalls whose distribution notice names Nebraska specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19851–19875 of 77956

  • HighNHTSA·22E083000·2022-09-29

    Chrysler Recalls Mopar Headlamp Assemblies for Dim Amber Reflectors

    Chrysler is recalling specific Mopar headlamp assemblies because the amber side reflex reflector may not reflect brightly enough, potentially reducing vehicle visibility.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V727000·2022-09-29

    2022 Lucid Air: Tow Eye Bracket Detachment Risk During Towing

    Lucid is recalling certain 2022 Air vehicles where the front tow eye bracket may be inadequately attached to the subframe and can detach during towing. This could separate the vehicle from the tow truck, increasing crash risk.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22780·2022-09-29

    Rockgeist BarJam Brackets Recalled Due to Crack and Injury Hazards

    Rockgeist BarJam Brackets can crack or break during use, causing gear to fall from a moving bicycle and posing crash and injury hazards. About 420 units sold online from September 2021 through August 2022.

    Product
    BarJam Brackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22232·2022-09-29

    North States Industries Recalls Toddleroo Rotating Cabinet Latches for Choking Risk

    North States Industries is recalling about 103,000 Toddleroo Rotating Cabinet Latches because the latching button can detach, posing a choking hazard to young children. The company has received 19 reports of the button dislodging, including one report of a child gagging.

    Product
    Toddleroo Rotating Cabinet Latches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22778·2022-09-29

    Hillsdale Furniture Flynn Twin Full Bunk Beds recalled for entrapment hazard

    Hillsdale Furniture is recalling about 821 Flynn Twin Full Bunk Beds With Ladders due to a gap wider than 3.5 inches between the second rung and lower bunk frame that poses an entrapment hazard to children when the mattress is removed. No injuries have been reported.

    Product
    Flynn Twin Full Bunk Beds With Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22779·2022-09-29

    E-Z-GO RXV Personal Transportation Vehicles Steering System Failure Recall

    Textron Specialized Vehicles recalled about 34,000 E-Z-GO RXV personal transportation vehicles (golf carts) because steering knuckles and A-arms can break during impact, causing loss of steering control and crash hazards.

    Product
    E-Z-GO RXV Personal Transportation Vehicles (PTV)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22233·2022-09-29

    Children's Bowtie Hairclips Recalled for Excessive Lead Content

    BE Jewel Accessories is recalling about 1,200 children's bowtie hairclips sold nationwide because the crystals exceed federal lead content limits. Lead poses a toxicity risk if ingested by young children.

    Product
    Children's Bowtie Hairclips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V724000·2022-09-29

    Chevrolet Equinox and GMC Terrain driver seat frame bolt defect

    General Motors is recalling certain 2022-2023 Chevrolet Equinox and 2022 GMC Terrain vehicles due to a potential issue with the driver's seat frame. The seat may not properly restrain an occupant in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC EQUINOX, TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V726000·2022-09-29

    Keystone Travel Trailers Recalled for Loose Hydraulic Leveling Foot Pads

    Keystone is recalling certain 2020-2023 travel trailers because hydraulic leveling leg foot pads may become loose and separate from the vehicle. A separated foot pad can become a road hazard, increasing the risk of a crash.

    Product
    KEYSTONE — KEYSTONE ALPINE, FUZION, IMPACT, AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22237·2022-09-29

    HyperJuice 130W USB-C Battery Packs Recalled for Fire Hazard

    Hyper Products is recalling HyperJuice 130W USB-C Battery Packs because they can overheat while charging and pose a fire hazard. Two reports of overheating have resulted in smoke, melting, and property damage.

    Product
    HyperJuice 130W USB-C Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22781·2022-09-29

    Yamaha Viking Off-Road Side-by-Side Vehicles Recalled for Brake Hazards

    Yamaha is recalling about 330 Model Year 2022 Viking Off-Road Side-by-Side vehicles because improperly installed rear brake lines can leak brake fluid and reduce vehicle control, creating crash and injury hazards.

    Product
    Yamaha Viking Off-Road Side-by-Side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22236·2022-09-29

    HyperJuice Stackable GaN USB-C Chargers Recalled for Fire Hazard

    Hyper Products is recalling about 18,200 HyperJuice Stackable GaN USB-C Chargers (models HJ414 65W and HJ417 100W) because they can overheat and pose a fire hazard. No injuries have been reported.

    Product
    HyperJuice Stackable GaN USB-C Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1748-2022·2022-09-28

    ANKUR Golden Raisins Recalled for Undeclared Sulfites

    ANKUR Golden Raisins (14 oz, UPC 8904 1740 10327) have been recalled due to undeclared sulfites. The voluntary recall affects 485 cases distributed to multiple states.

    Product
    ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear plastic bag, 20 bags per wholesale case
    Category
    Food
    Distribution
    14 states
  • SevereNHTSA·22V722000·2022-09-28

    2023 Western Star 49X Trucks Recalled Due to Tie Rod Defects

    Certain 2023 Western Star and Freightliner trucks are being recalled because tie rod clamps may be improperly heat-treated and crack, potentially causing loss of steering control.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4700, 4900, 49X, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1764-2022·2022-09-28

    FDA expands recall: HLS Set Advanced 7.0 sterility barrier compromise

    Maquet Medical Systems USA has expanded a recall for HLS Set Advanced 7.0, a preconnected medical device used for heart and lung support, due to a potential breach in the sterility barrier that could compromise product sterility.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70105.2794. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1772-2022·2022-09-28

    Serological Test Positive Control Shows False Negative Results for Hepatitis B

    Randox Serology I Positive Control may test negative for Hepatitis B surface antigen (HBsAg) on certain analyzers despite being designed as a positive control, potentially affecting laboratory quality control procedures.

    Product
    The Randox Serology I Positive Control contains the following analytes in human based plasma: Anti HIV 1/2, Anti HTLV 1/2, Anti HCV, HBsAg, Anti HBc, and Anti Treponema pallidum IgG. The product is delivered as a liquid in a kit of 3 identical ready-to-use vials of 5 mL each.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1769-2022·2022-09-28

    Hemodialysis Water Purification Unit Recalled for Missing EMI Shielding

    Fresenius is recalling 24 units of the AquaC UNO H reverse osmosis unit because internal ethernet cables lack ferrite cores, compromising electromagnetic compatibility in hemodialysis water purification systems.

    Product
    AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-10VA-1 Vivonic Part Number: G02000970-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1765-2022·2022-09-28

    Medical device set recalled for potential sterility barrier compromise

    Maquet Medical Systems USA is recalling the BEQ-HLS 5050 (HLS Set Advanced 5.0) due to a potential breach in the sterility barrier that may compromise product sterility.

    Product
    BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70105.2797. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V721000·2022-09-28

    Rolls-Royce Phantom Headlight Coating Defect Recall

    BMW is recalling 2023 Rolls-Royce Phantom vehicles because headlights may lack metal coating, causing low beams to fail FMVSS 108 and increasing crash risk.

    Product
    ROLLS-ROYCE — ROLLS-ROYCE PHANTOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1776-2022·2022-09-28

    FDA Recalls Grappler Suture Anchors Due to Potential Breakage Risk

    Paragon 28, Inc. is recalling Grappler Suture Anchors (REF: P44-110-3010-SK, Lot 5007499) due to risk that the anchor may break upon insertion, potentially leaving debris in patients and delaying surgery.

    Product
    Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1767-2022·2022-09-28

    Medical Device Recall: CARDIOHELP HLS Set Advanced Sterility Barrier Breach

    Maquet Medical Systems is expanding its recall of the CARDIOHELP HLS Set Advanced due to a potential breach in the sterility barrier that could compromise product sterility, affecting 6,871 US units and 18,670 worldwide.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70106.9078. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1766-2022·2022-09-28

    HLS Set Advanced Sterility Breach Recall for Cardiac Support Equipment

    Maquet Medical Systems USA is recalling HLS Set Advanced 5050 units due to a potential breach in the sterility barrier. The defect may result in compromised product sterility for this cardiac and respiratory support equipment.

    Product
    BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70106.9077. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide