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.

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.

47251–47275 of 78397

  • SevereNHTSA·17V153000·2017-03-09

    Jaguar Recalls 2017 F-PACE Vehicles Due to Short Rear Driveshaft

    Jaguar is recalling 2017 F-PACE vehicles with automatic transmissions because a short rear driveshaft may separate, causing loss of drive power and increasing crash risk.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V155000·2017-03-09

    Airstream Recalls 2017 Base Camp Trailers Due to Tire Contact Risk

    Airstream is recalling 2017 Base Camp recreational trailers because heavy loads may cause tires to contact the wheel well liner, risking tire failure and crashes.

    Product
    AIRSTREAM — AIRSTREAM BASECAMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V156000·2017-03-09

    Gillig Recalls 2016-2017 Low Floor Buses for Wiper Arm Defect

    Gillig is recalling 2,732 Low Floor transit buses because wiper arms can crack and detach, reducing driver visibility and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17107·2017-03-09

    Pier 1 Imports Recalls Bistro Chairs Due to Fall Hazard

    Pier 1 Imports is recalling Neely and Dahlia bistro chairs because loose bolts can cause the legs to collapse, posing a fall hazard.

    Product
    Neely and Dahlia Bistro Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V157000·2017-03-09

    Manac Recalls 2016-2017 Van Trailers Due to Failing Rub Rail Rivets

    Manac is recalling 2016-2017 Van Trailers because aluminum rivets securing external rub rails may fail, allowing the rails to detach and become road hazards.

    Product
    MANAC — MANAC VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1550-2017·2017-03-08

    Larry The Cable Guy Potato Chips Recalled for Salmonella Risk

    Shearers Foods is recalling Larry The Cable Guy Biscuits & Gravy Thin Potato Chips because ingredients may be contaminated with Salmonella.

    Product
    Larry The Cable Guy Biscuits & Gravy Thin Potato Chips 3 oz bag UPC 7 67212 62423 & 8 oz bag UPC 7 67212 62461
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Drugs)·D-0505-2017·2017-03-08

    Pacific Medical Solutions Recalls Nano PNC Water Due to Bacterial Contamination

    Pacific Medical Solutions is recalling Nano PNC Water because it was marketed without FDA approval and tested positive for the bacterium variovorax paradoxus.

    Product
    Nano PNC Water, packaged in amber glass bottles, Rx only, ICRPstudy.com, Immune Cellular Restoration Program.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1548-2017·2017-03-08

    Deep River Sour Cream & Onion Chips Recalled for Salmonella Risk

    Shearers Foods is recalling Deep River Sour Cream & Onion Krinkle Kettle Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.

    Product
    Deep River Sour Cream & Onion Krinkle Kettle Chips 2 oz bag UPC 8 50668 00049 8 & 5 oz bag UPC 8 50668 00099 3
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1552-2017·2017-03-08

    Shearers Foods Recalls Nacho Cheese Tortilla Chips Due to Salmonella Risk

    Shearers Foods is recalling specific bags of nacho cheese tortilla chips because they contain ingredients from a supplier that may be contaminated with Salmonella.

    Product
    NACHO CHEESE TORTILLA CHIPS: Essential Everyday 1 oz bag (Multi-pak) UPC 4 13030 05979; Essential Everyday 1 oz bag UPC 4 13030 59821, 10 oz bag UPC 4 13030 37638 & Market Essential 11.5 oz bag UPC 9 84873 00119
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1549-2017·2017-03-08

    Shearers Foods Recalls Jalapeno White Cheddar Potato Chips Due to Salmonella Risk

    Shearers Foods is recalling Delish Jalapeno White Cheddar Potato Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.

    Product
    Delish Jalapeno' White Cheddar KETTLE COOKED FLAVORED POTATO CHIPS NET WT 8.5 oz (241g) bag CONTAINS: MILK, UPC 4 49022 83607 5
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1553-2017·2017-03-08

    Shearers Foods Recalls Spicy Nacho Cheese Tortilla Chips Due to Salmonella Risk

    Shearers Foods is recalling Spicy Nacho Cheese Tortilla Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.

    Product
    SPICY NACHO CHEESE TORTILLA CHIPS: Essential Everyday 10 oz bag UPC 0 41303 06389 7 & Market Essential 11.5 oz bag UPC 0 98487 30014 0
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Drugs)·D-0496-2017·2017-03-08

    United Exchange Recalls Non-Sterile Eye Wash Bottles Nationwide

    United Exchange Corporation is recalling 46,080 bottles of Eye Wash due to direct evidence of non-sterility contamination in two lots.

    Product
    EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1368-2017·2017-03-08

    Windstone Medical Packaging Recalls Shoulder Arthroscopy Packs Due to Sterility Risk

    Windstone Medical Packaging is recalling 606 Shoulder Arthroscopy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Shoulder Arthroscopy Pack, part number AMS2496(A Shoulder Arthroscopy Pack, part number AMS2496(B Shoulder Arthroscopy Pack, part number AMS2496(C Shoulder Arthroscopy Pack, part number AMS2609 Shoulder Arthroscopy Pack, part number AMS3857 Shoulder Arthroscopy Pack, part…
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Devices)·Z-1329-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Lap/Pelviscopy Pack, part number PSS3256(B
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Devices)·Z-1251-2017·2017-03-08

    Olympus Recalls URF-P6 Uretero-reno Fiberscopes Due to Tissue Trauma Risk

    Olympus is recalling URF-P6 and URF-P6R uretero-reno fiberscopes due to adverse events involving tissue trauma and stuck insertion tubes reported in similar devices.

    Product
    URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V152000·2017-03-08

    Hyundai Recalls Sonata Models Due to Front Seat Belt Defect

    Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles because front seat belt linkages may detach from anchor pretensioners, increasing injury risk in crashes.

    Product
    HYUNDAI — HYUNDAI SONATA HYBRID, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0499-2017·2017-03-08

    United Exchange Recalls Eye Wash Bottles Due to Sterility Concerns

    United Exchange Corporation is recalling 190,710 bottles of Eye Wash due to a lack of assurance of sterility. The product was distributed nationwide, in Puerto Rico, and in Guyana.

    Product
    EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0788-2017·2017-03-08

    Medtronic SynchroMed II Software Card Recall for Priming Bolus Function

    Medtronic is recalling 22,298 SynchroMed II software application cards to update the priming bolus function and pump labeling.

    Product
    Medtronic SynchroMed II Implantable Drug Infusion System. This system includes: Model 8870 Software Application Card, Model 8840 N'Vision Clinician Programmer, and Model 8637 SynchroMed II Implantable Drug Infusion Pump (supplied in 20 ml or 40 ml reservoir size.) Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1379-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.

    Product
    Upper Torso Tray, part number PSS1554(B
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Drugs)·D-0497-2017·2017-03-08

    United Exchange Recalls Eye Irrigating Solution Due to Sterility Concerns

    United Exchange Corporation is recalling 112,320 bottles of Eye Irrigating Solution because the product lacks assurance of sterility.

    Product
    Eye Irrigating Solution, 4 fl oz (118 mL) bottle, OTC, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0536-1083-97
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0498-2017·2017-03-08

    United Exchange Eye Wash Recalled Due to Lack of Sterility Assurance

    United Exchange Corporation is recalling 77,184 bottles of Eye Wash because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide, in Puerto Rico, and in Guyana.

    Product
    Eye Wash, 4 fl oz (118 mL) bottle, OTC, Distributed by: United Exchange Corp., 17211 Valley View Ave., Cerritos, CA 90703, Made in Korea, UPC Code: 780707005828
    Category
    Drug
    Distribution
    Distributed nationwide