The Recall Desk

State

Nebraska product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56226–56250 of 78407

  • HighFDA (Devices)·Z-2381-2015·2015-08-19

    Etac Relax Wall Mounted Shower Seat Recalled for Cracked Brackets

    Etac Supply Center Ab is recalling 13 units of the Etac Relax wall mounted shower seat due to reports of the wall bracket cracking or breaking.

    Product
    Etac Relax wall mounted shower seat The Etac Relax is a wall mounted shower seat designed as a seating and standing support for personal hygiene purposes for people with reduced mobility. The Etac Relax shower seat is used for sitting where space is restricted, and can be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2353-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Spring Arm Defect

    Trumpf Medical Systems is recalling 9,287 surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,iLED 3/5, User Manual #1558932. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2354-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Spring Arm Defect

    Trumpf Medical Systems is recalling TruLight 3000/5000 surgical lights because the front joint of the spring arm could break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruLight 3000/5000, User Manual #1528403. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2364-2015·2015-08-19

    Cadence Recalls Perfectum Tuberculin Glass Syringes Due to Misaligned Marks

    Cadence Inc. is recalling 766 non-sterile Perfectum Tuberculin Glass Syringes because graduation marks are not centered with numeric position marks.

    Product
    Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1321-2015·2015-08-19

    Sensodyne Toothpaste Recalled for Wood Fragments

    GlaxoSmithKline is recalling Sensodyne Complete Protection toothpaste because wood fragments were found in the product.

    Product
    SENSODYNE COMPLETE PROTECTION — SENSODYNE COMPLETE PROTECTION (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2351-2015·2015-08-19

    Remel Recalls PathoDx Strep B Grouping Latex Reagent

    Remel Inc is recalling PathoDx Strep B Grouping Latex because a reagent may cause weak reactions, potentially leading to failure to identify target species.

    Product
    PathoDx Strep B Grouping Latex, REF 62031, 3 ml packaged in plastic dropper bottle with a pink cap. Latex reagent for streptococcal group B; Identify beta-hemolytic streptococci of Lancefield Groups A, B, C, F and G from primary culture plates.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2375-2015·2015-08-19

    Advanced Sterilization Products Recalls STERRAD 100NX Wall Charts for Incorrect Instructions

    Advanced Sterilization Products is recalling 1,465 STERRAD 100NX wall charts because they contain incorrect instructions regarding instrument tray wrapping.

    Product
    Wall Chart for STERRAD 100NX System, P/N 10104. The STERRAD 100NX Sterilizer is designed for sterilization of both metal and nonmetal medical devices at low temperatures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2352-2015·2015-08-19

    Merit Medical Recalls ReSolve Locking Drainage Catheters Due to Labeling Discrepancy

    Merit Medical Systems is voluntarily recalling 950 ReSolve Locking Drainage Catheters because the unit labeling may not match the actual device in the package.

    Product
    ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are intended for percutaneous drainage of fluids from body cavities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1322-2015·2015-08-19

    Sensodyne Complete Protection Recalled for Wood Fragments

    GlaxoSmithKline is recalling Sensodyne Complete Protection toothpaste because wood fragments were found in the product. Consumers should stop using the affected tubes.

    Product
    SENSODYNE COMPLETE PROTECTION — SENSODYNE COMPLETE PROTECTION (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1319-2015·2015-08-19

    Biotene Sodium Fluoride Toothpaste Recalled for Wood Fragments

    GlaxoSmithKline is recalling Biotene toothpaste because wood fragments were found in the product. Consumers should stop using the affected tubes.

    Product
    BIOTENE — BIOTENE (SODIUM FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2376-2015·2015-08-19

    Biotronik Recalls Unapproved Pacemaker Programmer Software Versions

    Biotronik is recalling specific pacemaker programmer software versions because they are not approved for use in the United States.

    Product
    PSW 1203.U/1, PSW 1301.U, PSW 1307.U, PSW 1403.U, and PSW 1501.U Pacemaker Programmer software. Software approved for use with BIOTRONIK device programmers (trade names: Renamic and ICS 3000). Allows physicians to program devices to pace exclusively in the left ventricle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1320-2015·2015-08-19

    Biotene PBF Toothpaste Recalled for Wood Fragments

    GlaxoSmithKline is recalling Biotene PBF toothpaste because wood fragments were found when the product was extruded.

    Product
    biotene PBF Toothpaste (Plaque-Biofilm Loosening Formula), a) 4.3 oz. (121.9 g) tubes, (NDC 0135-0559-01), biotene¿ PBF Paste, b) 4.5 oz.(127.6 g) tubes, (NDC 0135-0490-02), Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1324-2015·2015-08-19

    Sensodyne Toothpaste Recalled Due to Wood Fragments

    GlaxoSmithKline is recalling 325,504 tubes of Sensodyne toothpaste because wood fragments were found when the product was extruded.

    Product
    SENSODYNE — SENSODYNE (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1317-2015·2015-08-19

    Biotene Gentle Mint Gel Recalled for Wood Fragments

    GlaxoSmithKline is recalling Biotene Gentle Mint Gel tubes because wood fragments were found in the product. Consumers should stop using the affected lots.

    Product
    biotene Gentle Mint Gel, 4.5 oz.(127.6 g) tubes, Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108, NDC 0135-0488-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2363-2015·2015-08-19

    Stryker Recalls Mispackaged Orthopedic Shoulder Trial Instruments

    Stryker is recalling 21 units of a shoulder trial instrument because the package contained the wrong part number.

    Product
    ReUnion TSA Shoulder System, Standard SR Humeral Head Trial, 48X18, Catalog number 5901-S-4818. Orthopedic manual surgical instrument. Howmedica Osteonics Corp. A Subsidiary of Stryker Corp. Stryker France Non-sterile Made in Cork Ireland
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2361-2015·2015-08-19

    Abbott Recalls i-Stat PT/INR Cartridges Due to Test Delays

    Abbott Point Of Care Inc. is recalling specific lots of i-Stat PT/INR Cartridges because they may generate excessive star outs, potentially delaying patient results.

    Product
    i-Stat PT/INR Cartridges List number 03P89-24 The cartridges are packaged in sealed pouches, one per pouch. There are 24 cartridges packed in a box. a prothrombin time test useful in monitoring patients receiving oral anticoagulation therapy such as coumadin or warfarin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1323-2015·2015-08-19

    Sensodyne Toothpaste Recalled Due to Wood Fragments

    GlaxoSmithKline is recalling Sensodyne toothpaste tubes because wood fragments were found in the product. Consumers should stop using the affected tubes.

    Product
    SENSODYNE — SENSODYNE (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1318-2015·2015-08-19

    Biotene Fluoride Toothpaste Recalled for Wood Fragments

    GlaxoSmithKline is recalling Biotene fluoride toothpaste because wood fragments were found in the product. Consumers should stop using the affected tubes.

    Product
    BIOTENE — BIOTENE (SODIUM FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2360-2015·2015-08-19

    Stryker Recalls Mislabelled Triathlon Tibial Inserts for Knee Replacement

    Stryker Howmedica Osteonics is recalling 26 Triathlon tibial inserts because one unit was found in a package labeled for a different catalog number.

    Product
    Triathlon PS X3 Tibial Insert; No. 3 Triathlon TS Plus Tibial Insert X3 Poly 19 mm Product Usage: The Triathlon PS X3 (posterior stabilized), cat no 5532-G-xxx and X3 TS (total stabilizing) Plus, cat. no. 5537-G-XXX, Tibial Inserts are used in TKA surgeries. During surgery…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2951-2015·2015-08-19

    Mason Vitamins Recalls Mislabeled Coenzyme Q-10 50 mg Softgels

    Mason Vitamins, Inc. is recalling 13,027 bottles of Coenzyme Q-10 50 mg softgels because some bottles were mislabeled with the wrong dosage.

    Product
    Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes ENERGY in all Body Cells***Dietary Supplement 30 SOFTGELS***."
    Category
    Food
    Distribution
    31 states
  • SevereNHTSA·15V527000·2015-08-18

    Starcraft Transit Bus Recall for Fire Risk from Wiring

    Forest River is recalling 32 Starcraft transit buses due to an improperly routed cable that may cause an electrical short and fire.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALL STAR XL, XLT, ALL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V529000·2015-08-18

    E-One Emergency Vehicles Recalled for Lighting and Siren Safety Defect

    E-One is recalling 2013-2016 Pumpers, Tankers, and Rescue vehicles because the master power switch does not link to the start circuit, allowing operation without lights or sirens.

    Product
    E-ONE — E-ONE RESCUE, TANKER, PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide