The Recall Desk

State

Nebraska product recalls

73,486 recalls have nationwide distribution and so reach Nebraska. 4,576 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,576
Critical
715
Severe
1,343
Most recent
2026-10-14

Of the 4,576 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,343 (29%) are Severe.

These figures cover only the 4,576 recalls whose distribution notice names Nebraska specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22726–22750 of 78062

  • HighFDA (Devices)·Z-0775-2022·2022-03-23

    Boston Scientific JAGTOME RX device recalled for sterile barrier breach

    Boston Scientific has recalled 2209 units of the JAGTOME RX medical device worldwide due to compromised sterility from a sterile barrier breach. The affected units were distributed across the US and more than 40 countries.

    Product
    JAGTOME RX 44-30-260-035 Material Number: M00573060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0807-2022·2022-03-23

    BioPlex 2200 Syphilis Calibrator Set Recall Due to Vaccine Interference and Reagent Stability Issues

    Bio-Rad Laboratories is recalling 724 BioPlex 2200 Syphilis Calibrator sets due to COVID-19 vaccine interference concerns and manufacturing problems with reagent stability. The recalled lots were distributed nationwide in the U.S. and internationally.

    Product
    BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0869-2022·2022-03-23

    Honey BBQ seasoning recalled due to undeclared wheat allergen

    PS Seasoning & Spices recalls Honey BBQ Snack seasoning (3,001 units) distributed to 28 states and Canada due to undeclared wheat. Consumers with wheat allergies should not use affected lots.

    Product
    Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456. 2. 685-B, Net Wt 5.25 lbs. (2.38kg). Part #020001457. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder…
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0795-2022·2022-03-23

    Lumbar Puncture Tray Adult recalled due to manometer failure and leaking

    Bard Peripheral Vascular Inc is recalling 8,630 lumbar puncture trays due to manometer failure causing leaking and mating issues. Devices were distributed nationwide in the U.S. plus Puerto Rico, Costa Rica, and Hong Kong.

    Product
    LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0791-2022·2022-03-23

    Lumbar Puncture Tray Pediatric Recalled Due to Manometer Failure

    Bard Peripheral Vascular Inc is recalling pediatric lumbar puncture trays due to manometer leaking and mating failures that could prevent proper pressure measurement during procedures.

    Product
    LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0781-2022·2022-03-23

    Boston Scientific RX Cholangiogram Kit Recall Due to Sterile Barrier Breach

    Boston Scientific is recalling RX Cholangiogram Kits because the sterile barrier has been breached, compromising the sterility of the devices. The affected kits were distributed worldwide.

    Product
    RX CHOLANGIOGRAM KIT - SINGLE Material Number: M00575240 M00575240 M00575280 M00575320 M00575360 M00575380 M00575400 M00575440 M00575480
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0766-2022·2022-03-23

    Boston Scientific recalls 68 medical devices with sterility breach

    Boston Scientific is recalling 68 JAGTOME REVOLUTION RX medical devices due to sterile barrier breach. The devices were distributed worldwide including throughout the US.

    Product
    JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0762-2022·2022-03-23

    HYDRATOME RX surgical device recalled due to sterile barrier breach

    Boston Scientific recalls 251 HYDRATOME RX 44-30MM/450CM units worldwide due to sterile barrier breach that compromises device sterility.

    Product
    HYDRATOME RX 44-30MM/450CM Material Number: M00583070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0790-2022·2022-03-23

    FDA Recalls Safe-T PLUS Pediatric Lumbar Puncture Tray Due to Manometer Failure

    Bard Peripheral Vascular Inc is recalling 20,400 Safe-T PLUS pediatric lumbar puncture trays due to manometer leaking and mating failures. The devices were distributed nationwide and internationally to healthcare facilities.

    Product
    Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0771-2022·2022-03-23

    Medical Device Recall: Boston Scientific JAGTOME RX Sterile Barrier Breach

    Boston Scientific is recalling 98 units of the JAGTOME RX 39-30-260-025 medical device due to compromised sterile barrier that affects device sterility. Units were distributed worldwide.

    Product
    JAGTOME RX 39-30-260-025 Material Number: M00573100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0778-2022·2022-03-23

    Boston Scientific JAGTOME RX Recalled for Sterile Barrier Breach

    Boston Scientific is recalling 96 units of JAGTOME RX medical devices due to a sterile barrier breach that compromises device sterility. Patients should contact their physician if they received this device.

    Product
    JAGTOME RX 49-30-260-035 Material Number: M00573020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0776-2022·2022-03-23

    Medical Device Sterile Barrier Breach: JAGTOME RX Recall

    Boston Scientific is recalling JAGTOME RX medical devices because the sterile barrier may be compromised, which could allow contamination. The recall affects 163 units distributed worldwide.

    Product
    JAGTOME RX 44-30-450-035 Material Number: M00573070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0787-2022·2022-03-23

    Sorin Centrifugal Pump CP5 Drive Unit missing electromagnetic shielding component

    LivaNova is recalling four Sorin Centrifugal Pump CP5 Drive Units because a ferrite ring on the power cable may be missing. The units were distributed in Florida, Texas, and Nebraska.

    Product
    Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5 System configuration. A cardiopulmonary bypass speed control device.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0788-2022·2022-03-23

    LYFO Disk Quality Control Product Recalled for Organism Mislabeling

    Microbiologics Inc recalls LYFO Disk lot 983-40-3 because it is labeled as Candida tropicalis but actually contains Yersinia enterocolitica. The mislabeling may cause laboratory quality control failures and delayed test results.

    Product
    LYFO Disk
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0805-2022·2022-03-23

    Calcium Alginate Wound Dressings Recalled for Incorrect Instructions

    CellEra LLC is recalling Vitale Silver calcium alginate dressings nationwide because packages contain incorrect Instructions for Use with language not approved by the FDA. The firm is providing replacement packages with corrected instructions.

    Product
    20548 Vitale Silver calcium Alginate Dressings 4x8, 5/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0870-2022·2022-03-23

    Seasoning Recall: Undeclared Wheat in Honey BBQ Snack Stick Seasoning

    PS Seasoning & Spices, Inc. recalled Honey BBQ Snack Stick Seasoning containing undeclared wheat, affecting approximately 10,441 units distributed across multiple U.S. states and Canada. Consumers with wheat allergies should not consume affected products.

    Product
    Honey BBQ Snack Stick Seasoning packaged in the following sizes: 1. 765-A, Net Wt 21 lbs. (9.52kg). Part #020001203. 2. 765-B, Net Wt 5.25 lbs. (2.38kg). Part #020001299. 3. 765-C, Net Wt 2.63 lbs (1.19kg). Part #020001513. Ingredients: Sugar, Salt, Dried…
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Food)·F-0872-2022·2022-03-23

    FDA Recalls Seasoning Product for Undeclared Wheat Allergen

    PS Seasoning & Spices, Inc. recalled Maplewood Meats Honey BBQ Stick Seasoning (lot 2022-53578) for undeclared wheat. The product was distributed across multiple U.S. states and Canada; consumers with wheat allergies should not use it.

    Product
    Maplewood Meats Honey BBQ Stick Seasoning Net Wt 21 lbs. (9.50kg). Part #180002067. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder, Monosodium Glutamate, Natural Smoke Flavor, Sodium Erythorbate (0.26%), Dried Molasses, Natural Flavors…
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Drugs)·D-0653-2022·2022-03-23

    hydrALAZINE HCl Tablets 10 mg Recalled for Failed Impurity Specifications

    The Harvard Drug Group is recalling hydrALAZINE HCl Tablets, USP, 10 mg due to failed impurity and degradation specifications detected during routine stability testing. The recall affects 5,953 cartons distributed nationwide.

    Product
    hydrALAZINE HCl Tablets, USP, 10 mg, 100 Tablets per carton (10x10 blister packs), Rx only, Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152 USA. NDC # 0904-6440-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0873-2022·2022-03-23

    WAP Honey BBQ Seasoning Recalled Due to Undeclared Wheat Allergen

    PS Seasoning & Spices, Inc. is recalling WAP Honey BBQ Seasoning because it contains undeclared wheat. Consumers with wheat allergies should not consume this product.

    Product
    WAP Honey BBQ Seasoning Net Wt 20.64 lbs. (9.36kg). Part #180002073. Ingredients: Raw Cane Sugar, Sea Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder, Dried Molasses, Natural Flavors.
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-0802-2022·2022-03-23

    Calcium Alginate Wound Dressings Recalled for Incorrect Instructions

    CellEra LLC is recalling Vitale Silver calcium alginate wound dressings nationwide due to incorrect instructions for use containing language beyond FDA-cleared content.

    Product
    20522 Vitale Silver calcium Alginate Dressings 2x2, 10/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0804-2022·2022-03-23

    Calcium alginate wound dressings recalled for incorrect instruction labeling

    CellEra LLC is recalling Vitale Silver calcium alginate dressings because the included Instructions for Use contain language exceeding FDA clearance. The firm is replacing affected units with correct instructions.

    Product
    20545 Vitale Silver calcium Alginate Dressings 4x5, 10/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0801-2022·2022-03-23

    Medical dressing recall issued due to incorrect instructions for use

    CellEra LLC recalls Vitale Silver calcium Alginate Dressing Ropes due to incorrect Instructions for Use in product packaging. The manufacturer is replacing affected units with corrected instructions.

    Product
    20500 Vitale Silver calcium Alginate Dressing Ropes, 5/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0803-2022·2022-03-23

    Medical device wound dressing recall for incorrect instructions

    CellEra LLC is recalling Vitale Silver calcium Alginate Dressings because product packages contain incorrect Instructions for Use with language beyond FDA 510(k) clearance scope. The firm is replacing affected units with correct instructions.

    Product
    20544 Vitale Silver calcium Alginate Dressings 4x4, 10/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V172000·2022-03-22

    Marion Body Works Recalls 2018 International SR525 Emergency Vehicle

    Marion Body Works is recalling one 2018 International SR525 emergency vehicle because the engine may overcome the parking brake, increasing crash risk.

    Product
    MARION BODY WORKS — MARION BODY WORKS INTERNATIONAL SR525
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V173000·2022-03-22

    Hi-Tech E.V.S. Recalls Spartan Emergency Vehicles for Display Defect

    Hi-Tech E.V.S. is recalling 2020 Spartan MetroStar and 2021 Spartan Gladiator emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    HI-TECH E.V.S. — HI-TECH E.V.S. SPARTAN METROSTAR, SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide