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.

55251–55275 of 78407

  • HighFDA (Devices)·Z-2823-2015·2015-10-07

    Medtronic Solera Screwdrivers Recalled for Tip Deformation Risk

    Medtronic Navigation is recalling 2,346 Solera screwdrivers used in spine surgery because specific conditions may cause the tips to deform or break.

    Product
    P/N: 9735023, DRIVER 9735023 SOLERA 5.5/6.0 MAS; P/N: 9735024, DRIVER 9735024 SOLERA 5.5/6.0 MAS CAN; P/N: 9735025, DRIVER 9735025 SOLERA 5.5/6.0 RMAS; P/N: 9735026, DRIVER 9735026 SOLERA 5.5/6.0 RMAS CAN; P/N: 9735027,DRIVER 9735027 SOLERA 5.5/6.0 FAS/SAS. The Medtronic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2822-2015·2015-10-07

    MicroAire LipoTower Recalled for Potential Electrical Shock Hazard

    MicroAire Surgical Instruments is recalling 168 LipoTower units due to a risk of electrical shock if internal lead wires detach and the ground connection fails.

    Product
    ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2826-2015·2015-10-07

    Ferno iNX Wheeled Stretcher Recalled for Telescoping Load Frame Defect

    Ferno-Washington Inc is recalling 72 Ferno iNX Wheeled Stretchers because hole elongation in the load frame may allow the retention pin to move.

    Product
    Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2821-2015·2015-10-07

    MicroAire LipoTower Recall Due to Electrical Shock Risk

    MicroAire Surgical Instruments is recalling three LipoTower units with aspiration pumps due to a potential risk of electrical shock if internal lead wires detach.

    Product
    ASP-1020 LipoTower with Aspiration Pump. Medical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2820-2015·2015-10-07

    Zimmer Recalls Guide Wires Due to Incorrect Expiration Date Labeling

    Zimmer, Inc. is recalling 112,568 sterile guide wires because the labels state a 10-year expiration date, while testing supports only 5 years.

    Product
    Zimmer Guide Wires for orthopedic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0004-2016·2015-10-07

    Lifeline Systems Recalls Philips GoSafe Mobile Help Button Due to Battery Issues

    Lifeline Systems is recalling 8,616 Philips GoSafe Mobile Help Button devices because irregular battery disconnection can cause charging issues.

    Product
    Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0005-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, DARK, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2819-2015·2015-10-07

    Sterilmed Recalls Reprocessed Zimmer Tourniquet Cuffs Due to Mislabeling

    Sterilmed is recalling 43 reprocessed Zimmer tourniquet cuffs because they are labeled as single hose but are actually dual hose devices.

    Product
    Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34" Single Hose Single Bladder Brown (PLC), 34", Model (Reprocessor) Number: ZIM60-7075-106, Reprocessed by Sterilmed. Products are individually packaged in a Tyvek¿/poly pouch. There are 5 pouches placed inside a casepack box.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0001-2016·2015-10-07

    Guthy-Renker Recalls Rodan & Fields Proactiv Foundation for Subpotent Salicylic Acid

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, FAIR, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2818-2015·2015-10-07

    Olympus Recalls Gastrovideoscope Due to Insufficient Cleaning Accessory Information

    Olympus is recalling 1,014 EVIS EXERA II Gastrovideoscopes because specific cleaning accessories required for reprocessing were not provided.

    Product
    EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180; designed for endoscopic real-time ultrasound imaging, ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0003-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, MEDIUM, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0004-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling specific lots of Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, TAN, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0002-2016·2015-10-07

    Rodan & Fields Proactiv Foundation Recalled for Subpotent Salicylic Acid

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, LIGHT, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D1834-2015·2015-10-07

    Apotex Recalls Verapamil Hydrochloride Extended-Release Tablets for Dissolution Failure

    Apotex Inc. is recalling 2,075 bottles of Verapamil Hydrochloride Extended-Release tablets, 240 mg, because one lot failed to meet dissolution specification limits.

    Product
    Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by Apotex Research Private Limited, Bangalore, Karnataka 560 099, India; Manufactured for: Apotex Corp., Weston, FL 33326. NDC 60505-2742-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V625000·2015-10-06

    Winnebago and Itasca Motorhomes Recalled for Liquid Propane Hose Fire Risk

    Winnebago is recalling 2013-2016 Era, Trend, Tour, Journey, and Itasca motorhomes because a liquid propane hose may harden and leak, increasing fire risk.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA TREND, TOUR, JOURNEY, ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E082000·2015-10-06

    Dorman Aftermarket Steering Shafts Recalled for Potential Separation Risk

    Dorman is recalling aftermarket steering shafts for 1995-2002 Ford, Mercury, and Lincoln vehicles because they may separate, causing loss of steering control.

    Product
    MERCURY — MERCURY, FORD, LINCOLN GRAND MARQUIS, CROWN VICTORIA, TOWN CAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V626000·2015-10-06

    Kia Recalls 2011-2013 Sorento for Brake-Shift Interlock Defect

    Kia is recalling 2011-2013 Sorento vehicles because the brake-shift interlock may fail, allowing the car to roll out of Park without the brake being pressed.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E083000·2015-10-06

    Meritor Recalls Axles Due to Loose Caliper Bolts

    Meritor is recalling specific axle assemblies because caliper bolts may not be properly tightened. This defect could cause the caliper to detach, reducing braking performance and increasing crash risk.

    Product
    SERVICE BRAKES, AIR:DISC:CALIPER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E080000·2015-10-05

    SAF-Holland Recalls Trailer Axles Due to Spindle Separation Risk

    SAF-Holland is recalling specific 5-inch tapered trailer axles because the wheel end may separate from the axle, increasing the risk of a crash.

    Product
    SUSPENSION:REAR:AXLE:SPINDLE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E081000·2015-10-05

    Hale K Gearboxes Recalled for Shifting Out of Gear in Fire Apparatus

    Hale Products Inc. is recalling K Gearboxes used in fire apparatus that may shift from road to neutral while in transit, potentially increasing crash risk.

    Product
    POWER TRAIN:MANUAL TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V623000·2015-10-05

    Daimler Recalls 2016 Thomas Built Buses Due to Engine Stalling Risk

    Daimler Trucks North America is recalling 2016 Thomas Built Bus Saf-T-Liner C2 school buses because the engine control module may short circuit, causing the engine to stall without warning.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V621000·2015-10-02

    Mazda Recalls 2015-2016 Mazda3 Vehicles for Fuel Tank Valve Defect

    Mazda is recalling 2015-2016 Mazda3 vehicles because a fuel tank shut-off valve defect may cause fuel leaks or engine stalls, increasing fire and crash risks.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide