The Recall Desk

State

Nebraska product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52451–52475 of 78404

  • ModerateFDA (Food)·F-1104-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches for Potential Adulteration

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1 x 18, 1 x 48, 1 x100, 36 x 4, Mighty Mango Fruit & Veggies on the Go, (Apple/Mango/ButternutSquash) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1119-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Yellow Carrot/Banana (Boatin' Banana) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1498-2016·2016-04-27

    Optovue iVue OCT Systems Recalled for Software Display Anomaly

    Optovue is recalling iVue and iVue 500 OCT systems due to a software anomaly that may display duplicate eye images instead of distinct right and left views.

    Product
    iVue and iVue 500 (now called iScan) OCT systems with software version 2016.0.0.127 (USA only) and 2016.1.0.127 (out of US) Opthalmic: iVue is a non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional and…
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Drugs)·D-0827-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination Risk

    Hospira is recalling 11,256 bags of Dextrose Injection, USP, 70% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 70%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7918-19, Barcode (01) 0 030409 791819 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1114-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Pumpkin Spice Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1523-2016·2016-04-27

    Biocare Medical Recalls Mislabeled Mach 4 Mouse Probe Vials

    Biocare Medical is recalling a single lot of Mach 4 Mouse Probe vials that may be mislabeled as HRP-Polymer.

    Product
    Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit; Catalog number M4U534L; For In Vitro Use Immunology: MACH 4 Universal HRP-Polymer is a horseradish peroxidase (HRP)-antibody conjugate system intended for use in the detection of mouse lgG and lgM, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1116-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Peach/SweetPotato (Pedal Pedal Peach) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1110-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, 6 x 12, Apple/Grape Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateNHTSA·16T006000·2016-04-27

    Pirelli Recalls Tires Missing Required Date Codes

    Pirelli is recalling specific P Zero Trofeo tires that may lack required date codes, which could hinder identification during safety issues.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1108-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, Apple/Banana Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1517-2016·2016-04-27

    Stryker GDC 360 Detachable Coils Recalled for Incorrect Device Formulation

    Stryker Neurovascular is recalling 316 GDC 360 Detachable Coils because an incorrect Device Formulation Unit (DFU) was packaged with the product.

    Product
    GDC-18 360 11MM X 30CM Detachable Coil Sterile; Model number: M0033471020SR0 Neurology: GDC 360 degree Detachable Coils are intended for embolization of those intracranial aneurysms that¿a because of their morphology, their location, or the patients general medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1118-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Grape/Sweet Potato (Grateful Grape) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1522-2016·2016-04-27

    Abbott Recalls CELL-DYN Emerald Cleaner Due to Analyzer Quality Control Issues

    Abbott Laboratories is recalling CELL-DYN Emerald Cleaner because it may cause the hematology analyzer to generate out-of-range quality control results for RBC and PLT.

    Product
    CELL-DYN Emerald Cleaner, product number 09H46-02. 960mL. IVD; Hematology: The CELL-DYN Emerald Cleaner is designed for use on the CELL-DYN Emerald System, which is an automated hematology analyzer designed for in-vitro diagnostic use in clinical laboratories. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1111-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, 6 x 12, Apple/Mango Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0830-2016·2016-04-27

    Hospira Recalls Aminosyn-PF Amino Acid Bags Due to Chemical Contamination

    Hospira Inc. is recalling 1,776 bags of Aminosyn-PF (amino acids) 7% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Aminosyn-PF (amino acids) 7%, Sulfite-Free, 500 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 0409-4178-03 Barcode (01) 0 030409 417803 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1120-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 4 x 16, 120 x 12, 180 x 4, 360 x 4, 6 x 12, 7/16, 1 x 20, 1 x 24, and 36 x 4; Variety Packs/Multi-Packs with Multiple Flavor Varieties
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1107-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1x18, 4 x16, Apple/Cinnamon Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1509-2016·2016-04-27

    OraSure Recalls OraQuick HCV Visual Reference Panel Due to Incorrect Insert

    OraSure Technologies is recalling 244 OraQuick HCV Visual Reference Panel kits because the package insert may be incorrect, potentially containing instructions for a different test.

    Product
    OraQuick HCV Visual Reference Panel Intended to assist new operation in becoming proficient at reading specimens with antibody levels near the limit of detection of the device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0824-2016·2016-04-27

    Telmisartan Tablets Recalled Due to Presence of Silicone Foreign Matter

    Torrent Pharmaceuticals is recalling Telmisartan 80 mg tablets because a product complaint identified silicone foreign matter within the tablets.

    Product
    Telmisartan Tablets, USP, 80 mg, 30-count (3 x 10 unit-dose blisters) per carton, Rx only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, Dist. Mehsana, INDIA.; For: Torrent Pharma Inc., 150 Allen Road, Suite 102, Basking Ridge, NJ 07920, NDC 13668-158-72, UPC 3…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V246000·2016-04-26

    Ford Recalls 2016 F-Series Trucks for Tire Sidewall Damage

    Ford is recalling 2,288 model year 2016 F-250, F-350, F-450, and F-550 trucks because tires may have inner sidewall damage that could cause a blowout.

    Product
    FORD — FORD F-350 SD, F-550 SD, F-450 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V245000·2016-04-26

    Ford Recalls 2014-2015 Explorers for Rear Suspension Defect

    Ford is recalling 2014-2015 Explorers because rear suspension toe links may fracture, potentially causing loss of steering control and increasing crash risk.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V242000·2016-04-26

    Nissan Recalls 2013-2016 Sentra for Front Passenger Air Bag Defect

    Nissan is recalling 2013-2016 Sentra vehicles because a deformed seat belt bracket may prevent the front passenger air bag from turning off when a child seat is installed.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V241000·2016-04-26

    Toyne Recalls 2014-2015 Pumper Trucks Due to Gearbox Shift Defect

    Toyne Inc. is recalling 2014-2015 Pumper emergency vehicles because a gearbox defect may cause the truck to shift into neutral while driving, increasing crash risk.

    Product
    TOYNE — TOYNE PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V244000·2016-04-26

    Nissan and Infiniti Recall Vehicles Due to Passenger Air Bag Defect

    Nissan is recalling specific 2013-2017 Nissan, Infiniti, and Chevrolet vehicles because the passenger air bag may fail to deploy in a crash.

    Product
    NISSAN — NISSAN, INFINITI, CHEVROLET MURANO HYBRID, QX60 HYBRID, Q50 HYBRID, PATHFINDER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide