The Recall Desk

State

Nebraska product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31376–31400 of 78302

  • ModerateFDA (Devices)·Z-1624-2020·2020-04-08

    Gentell Hydrogel Ag Gauze Recalled for FDA Registration Deficiency

    Gentell, Inc. is recalling 20,025 units of Gentell Hydrogel Ag 4x4 gauze because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 4x4, model no. GEN-11420 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1600-2020·2020-04-08

    Butterfly iQ Ultrasound System Auto Bladder Volume Tool Recalled for Regulatory Violation

    Butterfly Network, Inc. is recalling the Butterfly iQ Ultrasound System Auto Bladder Volume Tool because it was distributed without an approved 510(k).

    Product
    Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder Volume Tool is a segmentation measurement tool REF/Model: 850-20003 Software versions 1.13.0, 1.14.0, and 1.15.0 - Product Usage: Butterfly iQ is indicated for use by qualified and trained healthcare…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1612-2020·2020-04-08

    Trilliant Surgical Recalls Instructions for Use for Cannulated Screw Systems

    Trilliant Surgical, LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for two cannulated screw systems to update dry time parameters.

    Product
    Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Ltd Tiger Large Cannulated Screw System, Model 215-00-001; and (2) Trilliant Surgical Ltd Large Cannulated Headless Screw System, Model 215-00-001. The firm name on the…
    Category
    Medical Device
    Distribution
    29 states
  • LowFDA (Drugs)·D-1258-2020·2020-04-08

    Akorn Recalls Fentanyl Citrate Injection Due to Impurity Specification Failure

    Akorn Inc. is recalling Fentanyl Citrate Injection, USP, 100 mcg/2 mL, because retained sample testing showed total impurities exceeded the allowed limit.

    Product
    Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 10 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1625-2020·2020-04-08

    Gentell Hydrogel Ag Saturated Gauze Recalled for FDA Registration Deficiency

    Gentell, Inc. is recalling 6,433 units of Gentell Hydrogel Ag Saturated Gauze because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1626-2020·2020-04-08

    Gentell Hydrogel Ag Wound Dressing Recalled for Registration Issues

    Gentell, Inc. is recalling Gentell Hydrogel Ag wound dressings because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 4oz. Tube, model no. - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Silver Antimicrobial Wound Dressing is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V201000·2020-04-07

    Vac-Tron Recalls Vacuum Excavator Trailers for Lighting Defects

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper lighting and missing reflectors may reduce visibility at night, increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MC 535, MC 533 SDT, MINICOMBO, MC 573 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V204000·2020-04-07

    Vac-Tron Recalls 2012-2020 Vacuum Excavator Trailers for Lighting Defects

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper exterior lighting and missing reflectors may reduce visibility at night, increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MC 873 SDT, MC 855 SDT, MC 833 SDT, MC 835 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V198000·2020-04-06

    KTM Recalls 2019-2020 790 Adventure Models Due to Rear Brake Hose Overheating

    KTM is recalling 2019-2020 790 Adventure and 790 Adventure R motorcycles because the rear brake hose may overheat, potentially causing brake failure and increasing crash risk.

    Product
    KTM — KTM 790 ADVENTURE R, 790 ADVENTURE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V193000·2020-04-03

    Isuzu Recalls 2019 NPR Vehicles Due to Brake Line Clip Defect

    Isuzu is recalling 2019 NPR and Chevrolet 4500 vehicles because incorrectly installed brake line clips may cause rear driver-side brake failure.

    Product
    ISUZU — ISUZU NPR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V196000·2020-04-03

    Trans Tech Bus Recalls 2020 Models for Seatbelt Warning Light Defect

    Trans Tech Bus is recalling 446 specific 2020 Roadstar, SST, and ST Aero buses because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition.

    Product
    TRANS TECH — TRANS TECH ROADSTAR, SST, ST AERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V190000·2020-04-02

    Setra S417TC Coaches Recalled for Front Door Detachment Risk

    Daimler Coaches is recalling 2017-2020 Setra S417TC coaches because the front entrance door support frame may be the wrong size, allowing the door to detach while moving.

    Product
    SETRA — SETRA S417 TC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20102·2020-04-02

    Manhattan Toy Recalls Musical Lili Llama Due to Choking Hazard

    Manhattan Toy is recalling Musical Lili Llama wooden activity toys because loose screws can fall off, posing a choking hazard to young children.

    Product
    Musical Lili Llama
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20104·2020-04-02

    VP Harrier and Giant Pinner DH Bicycle Pedals Recalled for Fall Hazards

    VP Components is recalling Harrier and Giant Pinner DH bicycle pedals because the spindle can separate from the pedal body, posing fall and injury hazards.

    Product
    VP Harrier and Giant Pinner DH bicycle pedals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20105·2020-04-02

    Stelpro Recalls Sonoma Wall Fan Heaters Due to Fire Hazard

    Stelpro Design is recalling about 3,600 Sonoma wall fan heaters because an internal part poses a fire hazard. Consumers should stop using the units and contact Stelpro for a free replacement.

    Product
    ASSO and ASSOS Sonoma wall fan heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V192000·2020-04-02

    KME Emergency Vehicles Recalled for Battery Corrosion Electrical Short Risk

    KME is recalling 2016-2020 emergency vehicles because battery corrosion can cause electrical shorts, potentially draining the battery and preventing operation during emergencies.

    Product
    KME — KME COMMERCIALCAB/ CHASSIS, PREDATOR PANTHER, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0886-2020·2020-04-01

    Clover Seed Recalled Due to Possible E. Coli Contamination

    International Sprout Holding Inc. is recalling clover seed in 50 lb. bags due to possible E. Coli contamination. The product was distributed to multiple states, territories, and countries.

    Product
    Clover seed in 50 lb. woven poly bags, 40 bags to a pallet.
    Category
    Food
    Distribution
    19 states