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.

46901–46925 of 78397

  • ModerateFDA (Devices)·Z-1703-2017·2017-04-05

    Siemens Dimension Vista Lab Systems Recalled for Potential ECREA Test Inaccuracy

    Siemens is recalling Dimension Vista 500 and 1500 lab systems because ECREA test results may be falsely elevated in isolated cases.

    Product
    Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Intelligent Lab System, analyzer, chemistry (photometric, discrete), for clinical use Product Usage: The Siemens Healthcare Diagnostics Dimension Vista System is an in vitro diagnostic device intended to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1736-2017·2017-04-05

    Give and Go Recalls Two-Bite Turtle Brownie Platters Due to Weevil Larvae

    Give and Go Prepared Foods is recalling Two-Bite Turtle Brownie Party Platters because dried weevil larvae may be present in the product.

    Product
    Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) item number 09904
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0617-2017·2017-04-05

    Zydus Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications

    Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed dissolution specifications and long-term stability testing.

    Product
    Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) and b) 500 count (NDC 68382-033-05) bottles, Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1688-2017·2017-04-05

    Siemens Syngo.x PACS Software Recalled for Addressing Multiple Issues

    Siemens Medical Solutions is recalling 104 Syngo.x PACS systems to install software updates that address several unspecified issues.

    Product
    Syngo.x, Picture archiving and communication system Syngo via is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a standalone device or together with a variety of cleared and unmodified syngo…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1689-2017·2017-04-05

    Siemens Syngo.via Software Recall for Medical Image System Issues

    Siemens Medical Solutions is recalling 104 units of Syngo.via picture archiving software to address several identified issues.

    Product
    Syngo.via, Picture archiving and communication system Syngo via is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a standalone device or together with a variety of cleared and unmodified syngo…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0624-2017·2017-04-05

    Sensodyne Toothpaste Recalled for Foreign Substance and Off-Flavor Complaints

    GSK Consumer Healthcare is recalling Sensodyne Repair & Protect Whitening toothpaste due to the presence of a foreign substance and low concentration of patchouli oil, causing off-flavor and scent complaints.

    Product
    SENSODYNE — SENSODYNE (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1737-2017·2017-04-05

    Give and Go Recalls Pecan Tarts Due to Weevil Larvae

    Give and Go Prepared Foods is recalling Two-Bite Pecan Tarts because dried weevil larvae may be present in the product.

    Product
    Two-Bite Pecan Tarts Party Platter 16 x 16.2 (460g) item number 09877
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1681-2017·2017-04-05

    Merge Eye Care Systems Software Recall Due to Image Acquisition Failure

    Merge Healthcare is recalling Eye Care Systems software because incompatible versions prevent the downloading or acquisition of new images.

    Product
    Merge Eye Care Systems, consisting of Merge Eye Station, Merge Eye Care PACS, and Merge Eye Station Import Utility (ESIU).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1698-2017·2017-04-05

    AGFA DX-D100 X-Ray System Recalled for Missing Allen Wrench Storage Instructions

    AGFA Healthcare Corp. is recalling 308 DX-D100 Digital Radiography X-Ray Systems because the user manual did not specify where to store the Allen wrench used for manual movement.

    Product
    AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to aid the physician with diagnosis
    Category
    Medical Device
    Distribution
    35 states
  • LowFDA (Drugs)·D-0623-2017·2017-04-05

    Hetero USA Recalls Montelukast Sodium Tablets Due to Discoloration

    Hetero USA Inc. is recalling 65,664 bottles of Montelukast sodium tablets due to a complaint of blue spots and powder inside a sealed bottle.

    Product
    MONTELUKAST SODIUM — MONTELUKAST SODIUM (MONTELUKAST SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1738-2017·2017-04-05

    Give and Go Mini Pecan Tarts Recalled for Dried Weevil Larvae

    Give and Go Prepared Foods is recalling Mini Pecan Tarts because dried weevil larvae may be present in the product.

    Product
    The Bakery Mini Pecan Tarts Part Platter NET WT 16x 16.2 OZ (460g) item number 08535
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1735-2017·2017-04-05

    Give and Go Recalls Pecan Tarts Due to Potential Weevil Larvae

    Give and Go Prepared Foods is recalling specific pecan tart products because dried weevil larvae may be present.

    Product
    Two-Bite Pecan Tart 9.2 oz (261g) item number 02023; NL Two-Bite Pecan Tarts 24 x 9.2 oz (261g) item number 02046; Sweet P's Bake Shop Pecan Tarts NET WT 9.2 oz (261g) item number 13076
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V228000·2017-04-04

    McNeilus Refuse Trucks and Mixers Recalled for CNG Fitting Defect

    McNeilus is recalling 2014-2016 refuse trucks and mixers with Cummins CNG engines due to an incorrect fitting that may cause a gas leak, fire, or engine stall.

    Product
    MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER, STANDARD MIXER, REFUSE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V230000·2017-04-04

    Gulf Stream Amerilite Trailers Recalled for Incorrect Weight Placards

    Gulf Stream is recalling 2011-2017 Amerilite trailers because incorrect weight information on the Federal Placard may lead to overloading and increased crash risk.

    Product
    GULF STREAM — GULF STREAM AMERILITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17125·2017-04-04

    Fred Meyer Recalls Children's Hooded Sweatshirts and Bomber Jackets

    Fred Meyer is recalling approximately 48,000 children's hooded sweatshirts and girls bomber jackets because the zipper pull can detach, posing choking and laceration hazards.

    Product
    Children's zipper hooded sweatshirts and girls bomber jackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V225000·2017-03-31

    Ford Recalls 2017 F-250 Super Duty Trucks Due to Transmission Defect

    Ford is recalling 2017 F-250 Super Duty trucks because a damaged transmission part may cause unexpected vehicle movement while in Park, increasing crash risk.

    Product
    FORD — FORD F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V224000·2017-03-31

    Kia Recalls 2011-2014 Models Due to Engine Bearing Wear Risk

    Kia is recalling 2011-2014 Optima, Sorento, and Sportage vehicles because machining errors may cause premature engine bearing wear, potentially leading to engine seizure and increased crash risk.

    Product
    KIA — KIA OPTIMA, SPORTAGE, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V223000·2017-03-31

    KME Predator Fire Trucks Recalled for Front Suspension Ball Joint Defect

    KME is recalling certain Predator fire trucks because front suspension ball joints can loosen, potentially causing a loss of steering control.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR SS AERIAL, PREDATOR AERIAL, PREDATOR SS PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V221000·2017-03-31

    Yamaha Recalls 2015-2017 Motorcycles for Handlebar Holder Defect

    Yamaha is recalling 22,433 motorcycles because the lower handlebar holder may loosen, potentially causing a loss of vehicle control.

    Product
    YAMAHA — YAMAHA XSR900, FJ-09, FZ-09
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17118·2017-03-31

    Black+Decker Portable Table Saws Recalled for Stand Collapse Hazard

    Rexon is recalling Black+Decker portable table saws sold at Walmart because the stand can collapse, posing laceration and impact injury risks.

    Product
    Black+Decker portable table saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V222000·2017-03-31

    BMW Recalls 2016-2017 MINI Cooper Clubman Vehicles for Brake Light Defect

    BMW is recalling 2016-2017 MINI Cooper Clubman vehicles because the inner brake light may fail to illuminate when turn signals are active, increasing crash risk.

    Product
    MINI — MINI COOPER S, COOPER CONVERTIBLE, COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide