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.

31576–31600 of 78302

  • HighCPSC·20096·2020-03-19

    Thule Recalls Sleek Car Seat Adapters Due to Fall Hazard

    Thule is recalling Sleek Car Seat Adapters because plastic brackets can break, posing a fall hazard to infants. No injuries have been reported.

    Product
    Thule Sleek Car Seat Adapters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20099·2020-03-19

    Crate and Barrel Recalls Miles Glass Pitchers Due to Laceration Hazard

    Crate and Barrel is recalling Miles Glass Pitchers with Wood Lid because the handle can break, posing a laceration hazard. No injuries have been reported.

    Product
    Miles Glass Pitchers with Wood Lid
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20723·2020-03-19

    Plant Therapy Recalls Wintergreen Oils for Non-Child-Resistant Packaging

    Plant Therapy is recalling specific wintergreen essential oils and blends because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Plant Therapy Wintergreen, Organic Wintergreen, Muscle Aid Synergy Blend, Tingly Mint Synergy Blend, and Vein Aid Synergy Blend Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V166000·2020-03-19

    BMW Recalls Motorcycles Due to Unclear Brake Fluid Reservoir Cap Labeling

    BMW is recalling specific 2018-2020 motorcycles because the brake fluid reservoir cap may not clearly state the required fluid type, potentially leading to improper maintenance.

    Product
    BMW — BMW R NINE T SCRAMBLER, R NINE T RACER, R NINE T, R 1250 RS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E013000·2020-03-19

    BMW Recalls Motorcycle Brake Fluid Reservoir Caps for Labeling Defect

    BMW is recalling specific motorcycle brake fluid reservoir caps because they may not clearly state the required brake fluid type, potentially leading to improper maintenance.

    Product
    BMW — BMW R NINE T SCRAMBLER, R 1250 R, R 1250 RS, R NINE T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20726·2020-03-19

    Kawasaki Recalls MULE PRO Utility Vehicles Due to Steering Shaft Wear

    Kawasaki is recalling approximately 80,000 MULE PRO off-highway utility vehicles because excessive steering shaft wear can affect steering control, posing a crash hazard.

    Product
    Kawasaki MULE PRO off-highway utility vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V154000·2020-03-18

    Bentley Recalls Bentayga Vehicles Due to Third-Row Seat Belt Defect

    Bentley is recalling 2018-2020 Bentayga vehicles with third-row seats because the upper seat belt attachment may detach in a crash, increasing injury risk.

    Product
    BENTLEY — BENTLEY BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1476-2020·2020-03-18

    Qiagen Rotor-Gene Q Software Recall for Incorrect Concentration Reporting

    Qiagen is recalling Rotor-Gene Q instruments with software version 2.3.4 because a bug causes concentration results to be reported as logarithmic values, potentially leading to false negative test results.

    Product
    QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycling and real-time detection of PCR assays.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1003-2020·2020-03-18

    American Health Packaging Recalls Ranitidine Tablets Due to NDMA Levels

    American Health Packaging is recalling 53,619 cartons of Ranitidine Tablets, 150 mg, due to potential N-Nitrosodimethylamine (NDMA) amounts above FDA-established levels.

    Product
    Ranitidine Tablets, USP, 150 mg, 100 Tablets (10 tablets x 10 blister card), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC carton: 60687-322-01; NDC Unit Dose Card: 60687-322-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1010-2020·2020-03-18

    Redline Pharmacy Recalls Vancomycin Injectable Due to Processing Control Deficiencies

    Redline Pharmacy Solutions is recalling 3 doses of Vancomycin 900MG Injectable due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Vancomycin 900MG in 100ML 0.9% NACL Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1007-2020·2020-03-18

    Redline Pharmacy Recalls Morphine Sulfate Due to Processing Control Deficiencies

    Redline Pharmacy Solutions is recalling Morphine Sulfate 20 mg/mL intrathecal syringes due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Morphine Sulfate, 20 mg/mL intrathecal, 20 mL per syringe. Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1004-2020·2020-03-18

    Precision Dose Recalls Ranitidine Oral Solution Due to NDMA Impurity

    Precision Dose Inc. is recalling Ranitidine Oral Solution because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    Ranitidine Oral Solution, USP, 150 mg/10 mL, [10 mL x 30 Unit Dose Cups per case, NDC: 68094-204-62; 10 mL x 100 Unit Dose Cups per case, NDC: 68094-204-61; Unit Dose Cup NDC: 68094-204-59], Rx only, Precision Dose, Inc., South Beloit, IL 61080
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0817-2020·2020-03-18

    Tova Industries Recalls American Bounty Chili Mix Due to Metal Shavings

    Tova Industries is recalling American Bounty Chili Mix w/Beans because of possible metal shavings in an ingredient. The recall covers 225 cases distributed to 11 states and the UAE.

    Product
    American Bounty brand Chili Mix w/Beans, Item #46628, in 20.8 oz. metallic pouches, 6 pouches per case.
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-1011-2020·2020-03-18

    Redline Pharmacy Recalls Morphine Sulfate Due to Processing Controls

    Redline Pharmacy Solutions is recalling Morphine Sulfate (MITIGO) 5 mg/mL intrathecal syringes due to a lack of processing controls.

    Product
    Morphine Sulfate (MITIGO), 5 mg/mL intrathecal, 40 mL per syringe. Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1009-2020·2020-03-18

    Redline Pharmacy Recalls Ertapenem Injectable Due to Processing Control Issues

    Redline Pharmacy Solutions is recalling 8 doses of Ertapenem Injectable due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Ertapenem in 100ML 0.9% NACL 1GM Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0812-2020·2020-03-18

    Tova Industries Recalls Shaver Foods Gravy Beef Due to Metal Shavings

    Tova Industries is recalling Shaver Foods brand Gravy Beef because of possible metal shavings in the ingredient. The product was distributed to 11 states and the United Arab Emirates.

    Product
    Shaver Foods brand Gravy Beef, Item #35089, in 2 lb. metallic pouches, 12 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0814-2020·2020-03-18

    Tova Industries Recalls Shaver Foods Gravy Chicken Due to Metal Shavings

    Tova Industries is recalling Shaver Foods brand Gravy Chicken because it may contain metal shavings. The product was distributed to 11 states and the United Arab Emirates.

    Product
    Shaver Foods brand Gravy Chicken, Item #35213, in 2 lb. metallic pouches, 12 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1475-2020·2020-03-18

    Getinge 88-Series Washer Disinfectors Recalled for Chamber Leakage Risk

    Maquet Cardiovascular is recalling Getinge 88-Series washer disinfectors because ruptured spot welds may cause water leakage, posing slip and infection risks.

    Product
    Getinge 88-Series-washer disinfectors intended for cleaning, disinfection and drying Model Number: 88-5 Part Number: 88-103; 88-203
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1455-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Hypodermic Safety Needles

    Cardinal Health is recalling Monoject Hypodermic Safety Needles that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.

    Product
    Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide