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.

48451–48475 of 78397

  • SevereFDA (Devices)·Z-0701-2017·2016-12-14

    3M Recalls Universal Electrosurgical Pads Due to Unintended Material Defect

    3M is recalling Universal Electrosurgical Pads because an unintended process liner may impede the safe return of electrosurgical current, increasing the risk of patient burns.

    Product
    3M Universal Electrosurgical Pad, REF 9130 (100 pads / case) and 3M Universal Electrosurgical Pad with Cord, REF 9135-LP (40 pads / case) Product Usage: 3M Universal Electrosurgical Pads are designed to work with most electrosurgical unite (ESU) for virtually every…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0179-2017·2016-12-14

    North American Rescue Recalls K-9 Trauma Field Kits Due to Sterility Concerns

    North American Rescue LLC is recalling K-9 Trauma Field Kits because the manufacturer has concerns about the sterility of the included eye wash irrigating solution.

    Product
    K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V900000·2016-12-14

    Mercedes-Benz Recalls Vehicles for Potential Axle Bolt Fracture Risk

    Mercedes-Benz is recalling certain 2015-2016 models because axle bolts may not have been assembled correctly, potentially fracturing and causing vehicle instability.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ML250, AMG GL63, GL550, ML400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0180-2017·2016-12-14

    North American Rescue Recalls Amphibious Trauma Kits Due to Sterility Concerns

    North American Rescue is recalling Amphibious Trauma Kits because the manufacturer has concerns about the sterility of the eye wash solution.

    Product
    Amphibious Trauma Kit - Product Code 85-0639, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0175-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Range Trauma Kit Hardcases because the manufacturer has concerns about the sterility of the eye wash irrigating solution included in the kits.

    Product
    Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0609-2017·2016-12-14

    Calbee Recalls Black Pepper Green Pea Crisps Due to Undeclared Milk

    Calbee North America is recalling one lot of black pepper flavored green pea crisps because they may contain undeclared milk.

    Product
    HARVEST SNAPS, SNAPEA CRISPS, BLACK PEPPER FLAVORED GREEN PEA CRISPS, NET WT 3.3 OZ (93g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V899000·2016-12-14

    Mercedes-Benz Recalls Vehicles Due to Electric Power Steering Defect

    Mercedes-Benz is recalling specific 2013-2016 models because a steering control unit defect may cause loss of power steering assist or a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E350, S550, SL550, S600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0183-2017·2016-12-14

    North American Rescue Recalls USCG Boat Response Kits Due to Sterility Concerns

    North American Rescue LLC is recalling USCG Boat Response Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.

    Product
    USCG Boat Response Kit - Product Code 80-0353, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0671-2017·2016-12-14

    Mondelez Recalls Oreo Fudge Creme Cookies for Undeclared Milk Allergen

    Mondelez is recalling Oreo Fudge Creme cookies because milk is not listed on the ingredient label.

    Product
    Nabisco Oreo Fudge Creme Original Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026943
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0182-2017·2016-12-14

    North American Rescue Recalls Aid Backpack Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Aid Backpack Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.

    Product
    Aid Backpack Kit - Product Code 85-0917, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V897000·2016-12-14

    Triple E Recalls 2017 Serenity S24CB RVs Due to Wiring Fire Risk

    Triple E is recalling 18 model year 2017 Serenity S24CB recreational vehicles because an incorrectly connected circuit wire poses a fire risk.

    Product
    TRIPLE E — TRIPLE E SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V898000·2016-12-14

    KZRV Recalls 2016-2017 Durango and Venom Trailers for Door Hinge Defect

    KZRV is recalling 2016-2017 Durango and Venom trailers because rear cargo door hinges may have insufficient welds, causing the door to swing down with excessive force.

    Product
    KZRV — KZRV DURANGO, VENOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0176-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue is recalling specific Range Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.

    Product
    Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0674-2017·2016-12-14

    Plush Puffs Marshmallows Recalled for Undeclared Milk Allergen

    To Your Heart's Content is recalling Plush Puffs Marshmallows in Toasty Coconut flavor because the product contains undeclared milk.

    Product
    Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16E093000·2016-12-14

    MORryde Recalls Zero G Ramp Door Hinges Due to Insufficient Welds

    MORryde is recalling approximately 2,500 Zero G Ramp Door hinges manufactured between August 21, 2016, and December 12, 2016, because insufficient welds may cause the door to swing down with excessive force.

    Product
    STRUCTURE:BODY:DOOR:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0707-2017·2016-12-14

    Merge Healthcare Recalls eFilm Workstation Software Due to Measurement Errors

    Merge Healthcare is recalling eFilm Workstation software versions 2.1 through 4.1 because RF projection images may display incorrect measurements without a calibration indicator.

    Product
    Merge, eFilm Workstation and eFilm Lite eFilm Workstation with Modules is a software application that is used for viewing medical images. eFilm Workstation with Modules receives digital images and data from various sources (including but not limited to CT, MR, US, RF units…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0721-2017·2016-12-14

    RayStation Radiation Therapy Software Recalled for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation software versions 4.0, 4.5, 4.7, and 5.0 due to potential inaccuracies in proton dose calculations for specific treatment plans.

    Product
    RayStation 4.0, 4.5, 4.7 and 5.0; Radiation Therapy Treatment Planning System Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0693-2017·2016-12-14

    Philips Brilliance 64 CT Systems Recalled for Software Error

    Philips Medical Systems is recalling 184 Brilliance 64 CT systems worldwide due to a software error involving the filament on timer.

    Product
    Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient and…
    Category
    Medical Device
    Distribution
    46 states
  • HighNHTSA·16V896000·2016-12-14

    DRV Recalls 2017 Full House Trailers Due to Door Hinge Weld Defect

    DRV Suites is recalling 2017 Full House recreational trailers because rear cargo door hinge welds may be insufficient, causing the door to swing down with excessive force.

    Product
    DRV — DRV FULL HOUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0623-2017·2016-12-14

    Green Dirt Farm Sheep's Milk Cheese Recalled for Staphylococcus Aureus Contamination

    Green Dirt Farm is recalling "Dirt Lover" sheep's milk cheese due to Staphylococcus aureus contamination exceeding action limits.

    Product
    Green Dirt Farm "Dirt Lover" sheep's milk cheese packaged in cases of 8, 4-6 oz.. units, sold by case weight. Made by Green Dirt Farm, LLC, Weston, MO 64098.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0697-2017·2016-12-14

    Philips Ingenuity CT Systems Recalled for Software Timer Error

    Philips Medical Systems is recalling 371 Ingenuity CT systems worldwide due to a software error involving the filament on timer.

    Product
    Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient and…
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Food)·F-0622-2017·2016-12-14

    Green Dirt Farm Ruby Blended Milk Cheese Recalled for Staphylococcus Aureus

    Green Dirt Farm is recalling Ruby blended milk cheese due to Staphylococcus aureus contamination exceeding action limits.

    Product
    Green Dirt Farm "Ruby" blended milk cheese packaged in cases of 6, 10 - 12 oz.. units, sold by case weight. Made by Green Dirt Farm, LLC, Weston, MO 64098.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0696-2017·2016-12-14

    Philips Ingenuity Core 128 MRI Software Recall for Timer Error

    Philips Medical Systems is recalling 509 Ingenuity Core 128 MRI systems due to a software error involving the filament on timer.

    Product
    Ingenuity Core 128 728323
    Category
    Medical Device
    Distribution
    46 states