The Recall Desk

State

Nebraska product recalls

73,741 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.

Which agencies issued them

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40326–40350 of 78321

  • HighFDA (Drugs)·D-0934-2018·2018-07-25

    Avella Recalls Heparin Bags Due to Potential Leakage and Sterility Concerns

    Avella of Deer Valley is recalling 240 bags of Heparin 25,000 Units in 5% Dextrose due to potential bag leakage and lack of sterility assurance.

    Product
    HEPARIN 25,000 Units in 5% Dextrose (Heparin Sodium, USP 25,000 Units, 5% Dextrose Inj., USP 250 mL) Volume: 255 mL. Single dose bag. Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix AZ 85085. NDC 42852-729-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2466-2018·2018-07-25

    Ethicon Recalls Pronova Suture Due to Packaging Perforation Risk

    Ethicon is recalling 516 units of Pronova Suture Blue because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.

    Product
    PRONOVA SUTURE BLUE 122CM M1.5, D10189
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2453-2018·2018-07-25

    Ethicon Prolene Suture Recall Due to Packaging Perforation Risk

    Ethicon is recalling specific Prolene suture products because a packaging design issue may allow needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE 36"(90CM) 4-0 BLUE, D7768
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2449-2018·2018-07-25

    Ethicon Proline Suture Recall Due to Packaging Perforation Risk

    Ethicon is recalling 1,728 units of Proline suture because a packaging design issue allows needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE BLUE 4X90CM M1.5 USP 4/0 DA RB-1 +P, D5981
    Category
    Medical Device
    Distribution
    25 states
  • HighNHTSA·18E061000·2018-07-25

    Rock Run Recalls LP Bottle Ring Brackets for Propane Tank Safety

    Rock Run Industries is recalling LP Bottle Ring Brackets that may break, potentially causing propane cylinders to fall from vehicles.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0948-2018·2018-07-25

    Avella Recalls Heparin Bags Due to Potential Leakage and Sterility Concerns

    Avella of Deer Valley, Inc. is recalling 40 bags of Heparin 1,000 Units in NS 250mL due to potential leakage that compromises sterility.

    Product
    HEPARIN 1,000 Units in NS 250mL. (Heparin Sodium, USP 1,000 Units, 0.9% Sodium Chloride, USP 250 mL) Volume: 251 mL. Single dose bag. For: Adventist Medical Center Hanford. By: Avella of Huston, 9265 Kirby Dr., Houston TX, 77054. NDC 42852-747-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2441-2018·2018-07-25

    Zeiss UV Disinfection Unit Recalled for Potential Radiation Exposure

    Zeiss is recalling 8 UV disinfection units for the Celldiscoverer 7 microscope because a firmware issue may allow the unit to activate outside its housing, exposing users to harmful UV radiation.

    Product
    Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2507-2018·2018-07-25

    Medtronic Tri-Staple 2.0 Reloads Recalled for Missing Sled Component

    Medtronic is recalling Tri-Staple 2.0 Black Intelligent Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.

    Product
    Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling system 60 mm Extra Thick, Item Code SIG60AXT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2454-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling 588 units of Proline Suture Blue 4x18" 5/0 due to a packaging design issue that may allow the needle to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE BLUE 4X18"5/0 DA RB-2 +PLG, D7879
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Drugs)·D-0949-2018·2018-07-25

    Avella Recalls Hydromorphone Syringes Due to Sterility Concerns

    Avella of Deer Valley is recalling 480 single-dose hydromorphone syringes due to potential bag leakage and lack of sterility assurance.

    Product
    HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg, 0.9% Sodium Chloride (USP) QS 30 mL) Volume: 30mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX. NDC 42852-222-63
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2452-2018·2018-07-25

    Ethicon Recalls Certain Proline Sutures Due to Packaging Design Issue

    Ethicon is recalling specific Proline sutures because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 30"(75CM) 4-0 BLUE, D7748
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2460-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Proline sutures because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.

    Product
    PROLENE SUTURE 4"(10CM) 8-0 BLUE, D9662
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2455-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue

    Ethicon, Inc. is recalling 432 units of Prolene Suture 30" 8-0 Blue (D8292) because the needle may perforate the packaging, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 30"(75CM) 8-0 BLUE, D8292
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2459-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue

    Ethicon, Inc. is recalling specific Prolene suture products because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 36"(90CM) 4-0 BLUE, D9067
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2451-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue

    Ethicon, Inc. is recalling specific Prolene suture products because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 4-36" (90CM) 3-0 BLUE, D6416
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2450-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue

    Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 4-36"(90CM) 4-0 BLUE, D5988
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2465-2018·2018-07-25

    Ethicon Recalls PRONOVA Suture Needles Due to Packaging Perforation Risk

    Ethicon is recalling specific PRONOVA suture needles because a packaging design issue may allow the needle to perforate the package, posing injury or infection risks.

    Product
    PRONOVA SUTURE BLUE MONO POLY - SH-1 Taperpoint 1/2C, D10027
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Drugs)·D-0930-2018·2018-07-25

    Avella Recalls Ephedrine Syringes Due to Potential Sterility Issues

    Avella of Deer Valley is recalling specific lots of ePHEDrine 50mg syringes because bags may leak, compromising sterility.

    Product
    ePHEDrine 50mg, 50 mg/10 mL (5 mg per mL) (Ephedrine Sulfate, USP 50mg in 0.9% Sodium Chloride, USPQS 10mL. 10 mL-Sterile use dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-805-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2458-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Proline sutures because a packaging design issue allows needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE 24"(60CM) 7-0 BLUE, D8881
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2461-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Prolene suture products because a packaging design issue may allow needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE BLUE 48" 4-0 D/A SH-1, D9746
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2463-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Proline suture products because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.

    Product
    PROLENE SUTURE MONO BLUE BV1755 Taperpoint 3/8C, D9995
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2479-2018·2018-07-25

    Hitachi Oasis MRI Systems Recalled for Exposed Belt Hazard

    Hitachi Medical Systems America Inc is recalling 264 Oasis MRI systems because an exposed stainless steel belt can cause finger cuts.

    Product
    Hitachi Oasis MRI system Product Usage: Hitachi MR system is an imaging device and is intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The Oasis system produces transverse…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0944-2018·2018-07-25

    Avella Recalls Fentanyl and Bupivacaine Cassettes Due to Sterility Concerns

    Avella of Deer Valley, Inc. is recalling 15 cassettes of fentanyl and bupivacaine due to potential bag leakage and lack of sterility assurance.

    Product
    fentaNYL 3 mcg/mL, 0.1% Bupivacaine, Fentanyl Citrate, USP 750 mcg, Bupivacaine HCL PF, USP, 250 mg, 0.9% Sodium Chloride, USP QS 250 mL. Volume: 250mL. Single dose Cassette. For: Methodist St. John Hospital, By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2467-2018·2018-07-25

    GE Medical Systems Recalls T2100 Microflex Drive Treadmill Units

    GE Medical Systems is recalling T2100 Microflex Drive Treadmills because unaddressed spare parts may cause uncontrolled walking belt motion during stress tests.

    Product
    T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Specifically the T210…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2464-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling 372 units of Proline Suture Blue 18" 7-0 because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.

    Product
    PROLENE SUTURE BLUE 18" 7-0 D/A BV-1, DC631
    Category
    Medical Device
    Distribution
    25 states