The Recall Desk

State

Nebraska product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49776–49800 of 78397

  • ModerateFDA (Drugs)·D-1522-2016·2016-10-05

    Pharmatech Recalls Ninjacof-A Liquid Due to Potential B. cepacia Contamination

    Pharmatech LLC is recalling Ninjacof-A liquid due to a potential risk of contamination with B. cepacia bacteria. This is a precautionary measure.

    Product
    Ninjacof-A (acetaminophen, chlophedianol HCl, pyrilamine maleate) Liquid, 160 mg/12.5 mg/12.5 mg in each 5 mL, 16 fl oz (473 mL) bottle, Manufactured for: Centurion Labs, LLC, Birmingham, AL 35243, NDC 23359-033-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2890-2016·2016-10-05

    EKOS Corporation Recalls EKOS Carts Due to Missing Wheel Washers

    EKOS Corporation is recalling 455 EKOS carts because missing washers may cause wheels to wear or dislodge, leading to equipment failure.

    Product
    The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/cart used to hold and transport the EkoSonic Control Unit. The cart is designed with three poles to hold infusion pumps and fluid bags, a tray on which the EkoSonic Control unit sits and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2899-2016·2016-10-05

    Siemens ADVIA Centaur Calibrator U Recalled for Analytical Sensitivity Failure

    Siemens is recalling ADVIA Centaur Calibrator U kits due to failure of analytical sensitivity and drift from internal standardization.

    Product
    Siemens ADVIA Centaur¿ Calibrator U, For in vitro diagnostic use in calibrating the following assays using ADVIA Centaur"' systems: Myoglobin cTnl Cat No. ADVIA Centaur Calibrator U (2 Pack) - 03684480 (SMN 1 0309996)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2897-2016·2016-10-05

    Prismatik Recalls BruxZir Shaded Dental Restorations Due to Quarantine Failure

    Prismatik Dentalcraft is recalling 150 units of BruxZir Shaded dental restorations because the manufacturer failed to properly identify quarantined lots as such.

    Product
    BruxZir Shaded, Model No. 70-1167-NOW0001, 70-1167-NOW0002, 70-1167-NOW0003, 70-1167-NOW0005, 70-1167-NOW0006 The device is indicated for use by dental technicians in the construction of custom made all ceramic restorations for anterior and posterior location.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1550-2016·2016-10-05

    Mckesson Recalls Mislabeled Lansoprazole Capsules Due to Labeling Error

    Mckesson Packaging Services is recalling 181 cartons of Lansoprazole capsules due to a label mix-up where the outer packaging was mislabeled.

    Product
    Lansoprazole Delayed-Release Capsules, USP, 30 mg, packaged in 100-count cartons of 10 x 10 unit dose blister cards, Rx only, Manufactured by: Dr. Reddy's Laboratories, Inc., 200 Somerset Corporate Blvd Floor 7, Bridgewater, NJ 08807, NDC 63739-0555-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2889-2016·2016-10-05

    Ethicon Mersilene Tape Recalled for Incorrect Instructions for Use Insert

    Ethicon, Inc. is recalling Mersilene Tape products because certain product codes were supplied with an incorrect Instructions for Use (IFU) insert.

    Product
    ETHICON MERSILENE" Tape (also referred to as MERSILENETM Polyester Fiber Strip or MERSILENETM Fiber Ligature)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1519-2016·2016-10-05

    Unichem Recalls Lamotrigine Tablets With Incorrect Imprint

    Unichem Pharmaceuticals is recalling 368 bottles of Lamotrigine 150 mg tablets because they have the wrong imprint. The FDA classifies this as Class III.

    Product
    LAMOTRIGINE — LAMOTRIGINE (LAMOTRIGINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·17004·2016-10-04

    Interlogix Recalls Wireless Personal Panic Devices Due to Operational Failure

    Interlogix is recalling about 67,000 wireless personal panic devices because they may fail to operate during an emergency. Consumers should contact their security installer for a free inspection and replacement.

    Product
    Interlogix ® wireless personal panic devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17003·2016-10-04

    Sargent Art Recalls Tempera and Finger Paints Due to Bacteria Risk

    Sargent Art is recalling 13 types of tempera and finger paints due to potential harmful bacteria. Consumers should stop using the products and contact the company for a refund.

    Product
    Arts and crafts tempera and finger paints
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V708000·2016-10-04

    REV Recalls 2010-2016 Road Rescue Vehicles Due to Touchscreen Software Defect

    REV is recalling 2010-2016 Road Rescue and other emergency vehicles because touchscreen software may cause accessories to turn on or off unexpectedly, increasing crash risk.

    Product
    ROAD RESCUE — ROAD RESCUE SPECIALTY VEHICLE, ULTRAMEDIC, TRANSMEDIC, DURAMEDIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17006·2016-10-04

    Office Depot Recalls Winsley Mid-Back Chairs Due to Fall Hazard

    Office Depot is recalling Winsley Mid-Back Chairs because they can tip over when users lean back, posing a fall hazard. No injuries have been reported.

    Product
    Winsley Mid-Back Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V705000·2016-10-03

    Kia Recalls 2016 Optima Vehicles Due to Front Axle Driveshaft Defect

    Kia is recalling 12,214 model year 2016 Optima vehicles because the right front axle driveshaft may crack and fail, potentially causing the vehicle to stop moving or roll unexpectedly.

    Product
    KIA — KIA OPTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V703000·2016-09-30

    AEV Traumahawk Ambulances Recalled for Defective Attendant Seat Tracks

    Halcore Group is recalling 2016-2017 AEV Traumahawk ambulances because defective seat tracks may cause the attendant seat to move rapidly during a crash, increasing injury risk.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V702000·2016-09-30

    MCI Recalls 2017 J4500 Motorcoaches Due to Brake Warning Defect

    Motor Coach Industries is recalling 2017 J4500 motorcoaches because a programming error may prevent low air pressure warnings, increasing crash risk.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V701000·2016-09-29

    Gillig Recalls 2016 Low Floor Buses Due to Axle Grease Defect

    Gillig is recalling 143 model year 2016 Low Floor transit buses because insufficient axle grease may cause bearing failure, increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16271·2016-09-29

    Walmart Recalls Tripod Stools Due to Fall Hazard

    Walmart is recalling Mahco Inc. tripod stools because the plastic collar connecting the legs can break, posing a fall hazard.

    Product
    Tripod stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E076000·2016-09-29

    Thieman Liftgates Recalled for Potential Roller Chain Failure

    Thieman is recalling specific liftgates because roller chains may fail, causing the platform to drop and increasing injury risk.

    Product
    STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide