The Recall Desk

State

Nebraska product recalls

73,381 recalls have nationwide distribution and so reach Nebraska. 4,575 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,575
Critical
715
Severe
1,343
Most recent
2026-09-23

Of the 4,575 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 4,575 recalls whose distribution notice names Nebraska specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19401–19425 of 77956

  • HighNHTSA·22V830000·2022-11-09

    2023 Volkswagen ID.4 electric motor coolant leak risk

    Volkswagen is recalling 2023 ID.4 vehicles due to improper electric motor sealing assembly that may allow coolant to leak into the high-voltage system, risking loss of vehicle control and unintended airbag deployment.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0122-2023·2022-11-09

    Cottage Cheese Products Recalled Due to Possible Plastic Contamination

    HP Hood LLC is recalling multiple cottage cheese brands (Hannaford, Hood, Market Basket, Weis) due to possible plastic fragments in the products. The recall affects 391,824 cases distributed across 38 states.

    Product
    Hannaford Fat Free Cottage Cheese, 16 oz and 24 oz; Hood Fat Free Cottage Cheese, 16 oz; Market Basket Fat Free Cottage Cheese, 16 oz and 24 oz; Weis Fat Free Cottage Cheese, 24 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0148-2023·2022-11-09

    Transcutaneous monitor attachment rings recalled for weak skin adhesion

    SenTec AG voluntarily recalled 17,208 units of transcutaneous CO2/O2 monitor attachment rings due to weak skin adhesion. The devices, used in noninvasive patient monitoring, were distributed nationwide.

    Product
    sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile skin. Used in continuous, noninvasive carbon dioxide and/or oxygen tension monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0130-2023·2022-11-09

    Hood Lowfat Cottage Cheese with Peaches Recalled for Plastic Foreign Objects

    HP Hood LLC recalls Hood Lowfat Cottage Cheese with Peaches due to possible plastic foreign objects. Affected products have best-by dates between October 24, 2022 and December 12, 2022.

    Product
    Hood Lowfat Cottage Cheese with Peaches
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0156-2023·2022-11-09

    Surgical Kit Sterile Pouches with Seal Openings Recalled by Medline

    Medline is recalling approximately 160 surgical kits with defective breather pouches showing seal openings, potentially compromising sterility. The recall affects facilities in eight states nationwide.

    Product
    BAUSCH + LOMB PHACO PACK, REF LYN011PHNHD. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0146-2023·2022-11-09

    Fogarty Arterial Embolectomy Catheters Recalled for Latex Deterioration

    Edwards Lifesciences is recalling 715,620 Fogarty Arterial Embolectomy Catheters due to confirmed latex deterioration in the pouch packaging. The material degradation could affect device performance during use.

    Product
    Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP 120807FP Fogarty Arterial Embolectomy Catheter with Stylet Model Number: 120403FSP 120803FSP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0169-2023·2022-11-09

    Cardiac Navigation Catheter Recalled for Cellulose Fiber Contamination

    Johnson & Johnson is recalling 91 THERMOCOOL SMARTTOUCH SF cardiac catheters nationwide due to manufacturing defects introducing cellulose fibers into the irrigation system. The contamination may prevent proper flushing, reduce cooling capability, or cause clotting complications.

    Product
    THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac electrophysiological mapping (stimulation and recording) and, in conjunction with an RF generator, for cardiac ablation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0167-2023·2022-11-09

    NICU PICC Insertion Bundle Recalled for Breather Pouch Seal Defects

    Medline Industries recalls NICU PICC insertion bundles (50 kits) due to openings in breather pouch seals that compromise sterile barrier integrity. This Class II recall affects units distributed across the United States.

    Product
    CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O, REF CVI4470. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0024-2023·2022-11-09

    Buprenorphine and Naloxone Sublingual Tablets Recalled for Foreign Substance

    Sun Pharmaceutical is recalling buprenorphine and naloxone sublingual tablets (8 mg/2 mg) due to a foreign substance. Affected lots DNC1129A and DNC1740A were distributed nationwide.

    Product
    BUPRENORPHINE AND NALOXONE — BUPRENORPHINE AND NALOXONE (BUPRENORPHINE AND NALOXONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0129-2023·2022-11-09

    Hood Lowfat Cottage Cheese recalled due to plastic foreign objects

    HP Hood LLC is recalling Hood Lowfat Cottage Cheese (16 oz and 24 oz) with best-by dates Oct 24–Dec 12, 2022, because the product may contain plastic foreign objects.

    Product
    Hood Lowfat Cottage Cheese, 16 oz and 24 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0163-2023·2022-11-09

    Medline LINQ Surgical Trays Recalled for Compromised Pouch Seals

    Medline has recalled LINQ TRAY surgical kits with breather pouch seal openings that could compromise sterility. The recall affects 40 kits distributed nationwide; no injuries have been reported.

    Product
    MEDLINE LINQ TRAY, REF DYNJ65880A. Convenience kit used in medical/surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0160-2023·2022-11-09

    Surgical Cataract Kits Recalled for Defective Breather Pouch Seals

    Medline has recalled Bausch + Lomb cataract surgical kits due to breather pouches with seal openings that could compromise sterility. Affected kits were distributed nationwide.

    Product
    BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0159-2023·2022-11-09

    Surgical eye kits recalled for breached sterile pouches

    Medline Industries recalls Bausch + Lomb eye muscle surgical kits due to breached breather pouches that may compromise sterility. The affected kits (Lot 22DBN366) were distributed nationwide.

    Product
    BAUSCH + LOMB EYE MUSCLE, REF VAL036EMESB. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0161-2023·2022-11-09

    Surgical Cataract Packs with Compromised Breather Pouch Seals Recalled

    Medline recalls 708 Bausch + Lomb cataract surgical packs due to breather pouch seal defects that could compromise sterility of surgical instruments.

    Product
    BAUSCH + LOMB CATARACT PACK, REF VAL001CPMEA. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0151-2023·2022-11-09

    Boston Scientific EMBLEM S-ICD Subcutaneous Defibrillators Software Defect Causes Battery Display Error

    Boston Scientific is recalling 7 EMBLEM S-ICD Model A209 subcutaneous defibrillators due to a software defect that displays inaccurate battery capacity information. Patients may not realize when their device's battery requires replacement.

    Product
    EMBLEM S-ICD, Subcutaneous Implantable Defibrillators, Model A209, sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0164-2023·2022-11-09

    Medline Dental Pack Recall Due to Breather Pouch Seal Defect

    Medline is recalling Dental Pack surgical kits (Lot 22DBE139) because breather pouches have openings in their seals that could compromise sterility. Affected units were distributed to healthcare facilities in eight US states.

    Product
    MEDLINE DENTAL PACK, REF DYNJ66983. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0155-2023·2022-11-09

    Surgical Eye Kit Pouches Recalled for Seal Defects

    Medline recalls Bausch + Lomb Eye surgical kits due to breather pouches with openings in the seal. Affected kits were distributed to healthcare facilities nationwide; unopened kits should not be used.

    Product
    BAUSCH + LOMB EYE PACK, REF LYN003EYSPA. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0166-2023·2022-11-09

    Medline CVC Barrier Kit Recalled for Breached Pouch Seals

    Medline is recalling CVC barrier kits (Lot 22ABT774) due to breather pouches with seal openings that could compromise sterility of the surgical kit contents.

    Product
    MEDLINE CVC BARRIER KIT, REF DYNJ80485. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0131-2023·2022-11-09

    Lactaid Cottage Cheese Recalled for Plastic Foreign Objects

    HP Hood LLC is recalling Lactaid Cottage Cheese (16 oz) with best-by dates Oct 24 2022 to Dec 12 2022 due to possible plastic contamination. Consumers should discard or return affected products.

    Product
    Lactaid Cottage Cheese, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0165-2023·2022-11-09

    Medline Radiology Procedure Pack Breather Pouches Recalled for Seal Defects

    Medline is recalling 240 Radiology Procedure Packs because some breather pouches show seal openings that could compromise sterility. The affected kits were distributed nationwide.

    Product
    MEDLINE RADIOLOGY PROCEDURE PACK, REF DYNJ67150A. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0128-2023·2022-11-09

    Hood Cottage Cheese with Pineapple Recalled for Possible Plastic Contamination

    HP Hood LLC is recalling Hood Fat Free Cottage Cheese with Pineapple, 16 oz containers for possible plastic contamination. Affected products have best-by dates from October 24, 2022 through December 12, 2022.

    Product
    Hood Fat Free Cottage Cheese with Pineapple, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Food)·F-0127-2023·2022-11-09

    Hood Everything Bagel Cottage Cheese Recalled for Plastic Fragments

    HP Hood LLC is recalling Hood Everything Bagel Cottage Cheese due to the potential presence of plastic fragments. The recall affects approximately 391,824 cases distributed across 37 states with best-by dates from October 24 to December 12, 2022.

    Product
    Hood Everything Bagel Cottage Cheese, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0152-2023·2022-11-09

    Implantable Defibrillator Software Error Causes Inaccurate Battery Display

    Boston Scientific's EMBLEM MRI S-ICD implantable defibrillators contain a software defect with an incorrect manufacturing date that causes inaccurate battery capacity display. The recall affects 142 devices distributed worldwide.

    Product
    EMBLEM MRI S-ICD, Subcutaneous Implantable Defibrillator, Model A219, sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0121-2023·2022-11-09

    Cottage Cheese with Pineapple Recalled for Plastic Contamination

    HP Hood LLC is recalling multiple brands of cottage cheese with pineapple due to possible plastic contamination. Products with best-by dates between October 24 and December 12, 2022 were distributed across 38 states.

    Product
    Food Club Cottage Cheese with Pineapple, 16 oz; Hannaford Cottage Cheese with Pineapple, 16 oz; Hood Cottage Cheese with Pineapple, 16 oz and 24 oz; Market Basket Cottage Cheese with Pineapple, 16 oz; Penn Maid Cottage Cheese with Pineapple, 16 oz;
    Category
    Food
    Distribution
    39 states