The Recall Desk

State

Nebraska product recalls

72,936 recalls have nationwide distribution and so reach Nebraska. 4,547 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,547
Critical
705
Severe
1,119
Most recent
2026-09-09

Of the 4,547 recalls naming Nebraska we have scored against our rubric, 705 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,119 (25%) are Severe.

These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3051–3075 of 77483

  • HighCPSC·26290·2026-02-26

    Bicystar High Chairs Recalled Over Fall and Entrapment Hazards

    About 150 Bicystar high chairs (model TB-HC6900) sold on Amazon are recalled because they lack the required crotch restraint and can trap a child's head, creating fall and entrapment hazards. No injuries have been reported.

    Product
    High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26298·2026-02-26

    TheKiddoSpace Recalls LED Soccer Hover Balls Due to Burn Hazard Risk

    TheKiddoSpace is recalling approximately 650 LED soccer hover balls because the battery surface temperature can exceed safety limits, posing a burn risk.

    Product
    TheKiddoSpace LED Soccer Hover Balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26303·2026-02-26

    Joyreal Busy Board Toys Recalled Over Choking and Laceration Hazards

    Joyreal Busy Board children's toys are recalled due to choking and laceration hazards from a detachable small mirror with sharp edges. No injuries have been reported.

    Product
    Joyreal Busy Board Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26306·2026-02-26

    Andersen Windows Recalls Window Opening Control Devices on 100 Series Casement Windows

    Andersen Windows is recalling about 91,000 window opening control devices sold as kits or installed on 100 Series casement windows because they can break or detach after impact, posing fall and serious injury hazards. No injuries have been reported.

    Product
    Window opening control devices sold as kits or installed on 100 Series casement windows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26278·2026-02-26

    PQL Recalls High Bay Linear LED Light Fixtures Due to Fire Hazard

    PQL recalls about 186,520 high bay linear LED light fixtures because degrading retaining pins can cause the LED board to come loose and spark a fire. One fire has been reported with no injuries.

    Product
    High Bay Linear LED light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26264·2026-02-26

    Vevor Retractable Baby Gates Recalled Due to Entrapment Hazard

    Sanven Technology is recalling approximately 10,400 Vevor Retractable Baby Gates because they violate safety standards and pose an entrapment risk to children.

    Product
    Vevor Retractable Baby Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26304·2026-02-26

    Concord Rechargeable Light-Up Bike Helmets Recalled Due to Head Injury Risk

    Todson is recalling about 40,245 Concord 360 Degree Rechargeable Light-Up Bike Helmets because they fail to meet safety standards, posing a risk of serious head injury or death.

    Product
    Concord 360 Degree Rechargeable Light-Up Bike Helmet
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V112000·2026-02-26

    Honda Prologue and Acura ZDX instrument and camera displays may fail

    Honda is recalling certain 2024 Acura ZDX and Prologue vehicles because a software error may cause the instrument panel display to fail and the rearview camera to show a blank screen in reverse.

    Product
    ACURA — ACURA, HONDA ZDX, PROLOGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26289·2026-02-26

    Magnetic Chess Games Recalled Over Magnet Ingestion Risk

    Magnetic chess games sold on Amazon by Kaiwenshangpin are recalled because loose magnets inside can be swallowed by children, potentially causing intestinal damage or death. No injuries have been reported.

    Product
    Magnetic Chess Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26293·2026-02-26

    TheKiddoSpace Recalls Children's Handwriting Kits Over Lead Exposure

    TheKiddoSpace is recalling about 19,700 children's handwriting practice kits because the pens contain lead levels that violate the federal lead content ban. No injuries have been reported.

    Product
    TheKiddoSpace Print and Cursive Handwriting Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26295·2026-02-26

    TheKiddoSpace Recalls Reusable Water Balloons Over Phthalate Ban Violation

    TheKiddoSpace is recalling about 4,300 reusable water balloons because the cord lock on the storage bag contains a regulated phthalate that violates the federal phthalate ban. No injuries have been reported.

    Product
    TheKiddoSpace Reusable Water Balloons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V115000·2026-02-26

    BMW Recalls One 2026 S 1000 RR Motorcycle for Turn Signal Defect

    BMW is recalling one 2026 S 1000 RR motorcycle because the turn signal reset button can be unintentionally activated, causing the turn signal to fail.

    Product
    BMW — BMW S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26292·2026-02-26

    TheKiddoSpace Recalls Children's Story Books Due to Choking Hazard

    TheKiddoSpace is recalling about 140 children's story books because felt parts can detach and pose a choking hazard. No injuries have been reported.

    Product
    TheKiddoSpace Children's Story Books
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26305·2026-02-26

    SumDirect LED Mini Lights Recalled Over Battery Ingestion Hazard

    SumDirect LED Mini Lights are recalled because the button cell batteries can be easily accessed by children, posing an ingestion hazard. No injuries have been reported.

    Product
    SumDirect LED Mini Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26302·2026-02-26

    Zelbuck Magnetism Ball Game Toys Recalled Due to Ingestion Hazard

    Zelbuck Magnetism Ball Game Toys are being recalled because they contain loose magnets that pose a serious injury or death risk if swallowed.

    Product
    Zelbuck Magnetism Ball Game Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V114000·2026-02-26

    General Motors Vehicles Recalled for Missing Electronic Owner's Manual

    General Motors has recalled multiple Chevrolet, GMC, Cadillac, and Buick vehicles from 2025–2027 because their radios were not properly configured to download the electronic owner's manual during production. Without the manual, owners may not know how to safely operate the vehicle.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, BUICK SILVERADO 2500, SILVERADO 3500, BLAZER EV, VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1353-2026·2026-02-25

    Olympus High Flow Insufflation Unit Model UHI-2 Recalled Due to Software Issue

    Olympus Corporation of the Americas is recalling 744 Olympus High Flow Insufflation Units (Model UHI-2) because a software algorithm issue may cause overpressure events.

    Product
    Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0510-2026·2026-02-25

    Moringa capsules recalled over potential contamination with Salmonella

    Art Monkey LLC is recalling 8,500 bottles of Why Not Natural Moringa Capsules because they have the potential to be contaminated with Salmonella.

    Product
    Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1352-2026·2026-02-25

    Olympus High Flow Insufflation Unit Recalled Due to Software Algorithm Issue

    Olympus Corporation of the Americas is recalling the Olympus High Flow Insufflation Unit (Model UHI) because a software algorithm issue may cause overpressure events.

    Product
    Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1404-2026·2026-02-25

    Medline Burn Care Kits Recalled Over Sterilization Calibration Issues

    Medline is recalling 291 units of three burn care convenience kits due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.

    Product
    Medline Convenience Kits: 1) BURN PACK, Model Number: DYNJ15668R; 2) BURN PACK-LF, Model Number: DYNJ42829B; 3) BURN CARE PACK-LF, Model Number: DYNJT3437
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1415-2026·2026-02-25

    Medline Recalls Surgical Convenience Kits Over Sterilization Calibration Issues

    Medline is recalling 12,418 units of various surgical convenience kits due to calibration issues with equipment used for sterilization and packaging, which may affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) ROBOTIC GYN CDS-1, Model Number: CDS982893I; 2) GYN LAPAROSCOPY CDS, Model Number: CDS983300J; 3) NHP ROBOTIC GYNE CDS, Model Number: CDS984243G; 4) ROBOTIC-LF, Model Number: CDS984543D; 5) ROBOTIC-LF, Model Number: CDS984543F; 6) ROBOTIC-L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1385-2026·2026-02-25

    Medline Tracheostomy Convenience Kits Recalled Over Sterilization Calibration Concerns

    Medline is recalling 753 units of its tracheostomy convenience kits and trach tote due to potential sterilization equipment calibration issues that may affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55; 2) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55A; 3) TRACH TOTE, Model Number: DYNJ85691
    Category
    Medical Device
    Distribution
    Distributed nationwide