The Recall Desk

State

Nebraska product recalls

73,376 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.

Which agencies issued them

These figures cover only the 4,575 recalls whose distribution notice names Nebraska specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18926–18950 of 77951

  • HighFDA (Devices)·Z-0758-2023·2022-12-28

    Vivid i N ultrasound device batteries may fail, smoke, or catch fire

    GE Medical Systems recalls Vivid i N ultrasound machines worldwide because unreplaced batteries may fail, emit smoke, or catch fire. Users should replace batteries every 2 years per the service manual.

    Product
    Vivid i N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0762-2023·2022-12-28

    Baxter Revaclear 300 Dialyzers Recalled for Polyurethane Displacement

    Baxter is recalling approximately 14 million units of Revaclear 300 dialyzers worldwide due to polyurethane displacement that could cause blood leaks. No injuries have been reported.

    Product
    Revaclear 300 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0753-2023·2022-12-28

    GE Vivid S6 Ultrasound Systems Recalled for Battery Fire Risk

    GE Vivid S6 ultrasound systems are recalled for a potential battery hazard. If not replaced at the recommended 2-year interval, batteries may fail, emit smoke, or catch fire.

    Product
    Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0457-2023·2022-12-28

    SurfaceSoap UV Disinfecting Wand Recalled for Excessive Ultraviolet Radiation

    PhoneSoap has recalled its SurfaceSoap UV Disinfecting Wand due to excessive ultraviolet-C radiation emission. Approximately 6,700 units distributed nationwide may pose a radiation hazard to users.

    Product
    The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0089-2023·2022-12-28

    Quinapril Tablets Recalled Due to Excess Impurity Above Limits

    Lupin Pharmaceuticals is recalling Quinapril tablets (20 mg) due to N-nitroso-quinapril impurity detected above acceptable daily intake limits. The recall affects approximately 23,736 units distributed nationwide.

    Product
    QUINAPRIL — QUINAPRIL (QUINAPRIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0741-2023·2022-12-28

    InPen Diabetes App crashes, preventing dose reminders

    The InPen Diabetes Management App may crash on certain Android versions, preventing dose reminders and potentially delaying insulin therapy. This could affect users of the diabetes management system.

    Product
    InPen Diabetes Management App, part of the InPen System, REF: MMT-105ELBLNA, MMT-105ELGYNA, MMT-105ELPKNA, MMT-105ELPKNA, MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0085-2023·2022-12-28

    Oxcarbazepine 600mg tablets recalled for foreign substance contamination

    Sun Pharmaceutical is recalling three lots of Oxcarbazepine 600mg tablets due to the presence of foreign substances. The affected medication was distributed nationwide.

    Product
    OXCARBAZEPINE — OXCARBAZEPINE (OXCARBAZEPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0724-2023·2022-12-28

    DeVilbiss 525 Oxygen Concentrator Recalled Due to Excessive Heat

    DeVilbiss is recalling the 525 oxygen concentrator because the device can become excessively hot, with external parts potentially exceeding 105.8 degrees Fahrenheit. The firm has updated the user manual to include additional safety warnings.

    Product
    DeVilbiss, 525 5-liter Oxygen Concentrator Models 525DS, 525DS-Q
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0754-2023·2022-12-28

    Vivid S5 N Ultrasound Systems Recalled for Potential Battery Fire Hazard

    GE Medical Systems recalled 1,400 Vivid S5 N ultrasound systems for batteries that may fail, emit smoke, or catch fire if not replaced every 2 years as recommended.

    Product
    Vivid S5 N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0727-2023·2022-12-28

    Corin BIOLOX DELTA ceramic hip replacement heads mislabeled with incorrect sizes

    Corin Ltd is recalling BIOLOX DELTA ceramic hip replacement heads because some units are labeled with incorrect sizes. The recall affects 12 units distributed in seven U.S. states.

    Product
    Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0725-2023·2022-12-28

    Intradental periodontal picks recalled for mislabeling by Young Dental

    Young Dental Manufacturing has recalled Denticator PICK-A-DENT intradental picks due to mislabeling. The recall affects 600 packs distributed in Iowa, New York, Pennsylvania, Tennessee, Texas, and Canada.

    Product
    Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V955000·2022-12-23

    Mercedes-Benz Recalls GLE and ML Models for Fuel Pump Water Damage

    Mercedes-Benz is recalling 2012-2020 GLE and ML models because water in the spare tire well can damage the fuel pump control unit, causing engine stalls.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ML350, ML550, ML250, AMG ML63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V954000·2022-12-23

    Mercedes-Benz Recalls Vehicles Due to Sunroof Panel Detachment Risk

    Mercedes-Benz is recalling 2001-2011 C, CLK, E, and CLS class vehicles because the glass sunroof panel may detach, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ AMG E63, CLK500, CLS550, E550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V953000·2022-12-23

    2020-2023 Lincoln Aviator and Corsair Seat Belt Warning Chime Duration Defect

    Ford is recalling certain 2020-2023 Lincoln Aviators and Corsairs because the seat belt warning chime may activate for less than 4 seconds, failing to properly alert unbelted drivers.

    Product
    LINCOLN — LINCOLN AVIATOR, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E101000·2022-12-23

    Warn Industries Recalls Winch Remotes Due to Water Intrusion Risk

    Warn Industries is recalling wireless winch remotes because water intrusion can cause corrosion, leading to unintentional winch operation and injury risk.

    Product
    EQUIPMENT:MECHANICAL:WINCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23078·2022-12-22

    Target Recalls Pillowfort Weighted Blankets Due to Asphyxiation Risk

    Target is recalling about 204,000 Pillowfort Weighted Blankets because children can become entrapped inside the blanket cover, creating a risk of asphyxiation. Two children have died from this hazard.

    Product
    Pillowfort™ Weighted Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·045-2022·2022-12-22

    Morasch Meats Recalls Raw Frozen Diced Beef Due to E. Coli O157:H7

    Morasch Meats is recalling approximately 3,930 pounds of raw frozen diced beef products produced on August 24, 2022, due to possible E. coli O157:H7 contamination.

    Product
    Morasch Meats, Inc — Morasch Meats Inc. Recalls Raw Frozen Diced Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·23080·2022-12-22

    Samsung Top-Load Washing Machines Recalled for Fire Hazard

    Samsung has recalled about 663,500 top-load washing machines because the machines can short-circuit and overheat, posing a fire hazard. A free software update is available to resolve the issue.

    Product
    Samsung Top-Load Washing Machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V951000·2022-12-22

    Motorhomes recalled for faulty LPG service valves causing propane leak risk

    Kibbi is recalling 2022–2023 Renegade Valencia motorhomes. Service valves on LPG tanks may be improperly connected, creating a propane leak risk that could lead to fire if an ignition source is present.

    Product
    RENEGADE — RENEGADE, RENEGADE RV VALENCIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V950000·2022-12-22

    2022 Acura TLX Tire Damage Recall Due to Bead Cuts and Tears

    Honda is recalling approximately 19 model-year 2022 Acura TLX vehicles because their tires may have sustained cuts and tears. Damaged tires can lead to loss of vehicle control and increase crash risk.

    Product
    ACURA — ACURA TLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23075·2022-12-22

    GASGAS Off-Road Motorcycles Recalled for Engine Failure and Crash Hazards

    KTM North America is recalling about 231 GASGAS MC 250 motorcycles due to an incorrectly programmed CDI box that can cause engine failure and pose crash and injury hazards. Consumers should stop riding the motorcycles immediately and contact an authorized dealer for a free repair.

    Product
    GASGAS Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23077·2022-12-22

    Pacific 20-Inch Kids' Bicycles Recalled for Loose Handlebar Fall Hazard

    Pacific Cycle is recalling about 147,000 Pacific Igniter and Pacific Bubble Pop 20-inch bicycles sold at Target because the handlebars can become loose during use, posing a fall hazard. Ten injuries involving bruising and abrasions have been reported.

    Product
    Pacific Igniter and Pacific Bubble Pop 20" kids' bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23076·2022-12-22

    BLU3 Nomad Battery-Powered Tankless Diving Systems Recalled for Drowning Hazard

    BLU3 is recalling about 1,300 Nomad battery-powered tankless diving systems because the compressor head can fracture during use, restricting airflow and posing a drowning hazard to divers. No injuries have been reported.

    Product
    Nomad Battery-Powered Tankless Diving Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V948000·2022-12-22

    Shadow Living Quarter Travel Trailers Recalled for Gas Leak Risk

    Shadow Trailer is recalling 2021-2022 Living Quarter travel trailers because damaged burner control valves may cause a gas leak, increasing fire risk.

    Product
    SHADOW — SHADOW LIVING QUARTER
    Category
    Vehicle
    Distribution
    Distributed nationwide