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.

50251–50275 of 78397

  • SevereNHTSA·16E069000·2016-08-29

    Idle Free Systems Recalls Auxiliary Power Units Due to Fire Risk

    Idle Free Systems is recalling 507 Auxiliary Power Units with Reefer-type trailer Link Kits manufactured between 2010 and 2016. The battery positive cable may short to ground, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V626000·2016-08-29

    KME Fire Trucks Recalled for Potential Driveshaft Failure

    Kovatch Mobile Equipment is recalling 56 KME fire trucks because replacement driveshafts may twist and fail, potentially immobilizing the vehicle.

    Product
    KME — KME PREDATOR SS PUMPER, FDNY PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·075-2016·2016-08-26

    WFSP Foods Recalls Pork and Chicken Sausage Due to Undeclared Milk Allergen

    WFSP Foods LLC is recalling approximately 18,672 pounds of Land O Frost sausage products because the packaging fails to declare milk, a known allergen.

    Product
    WFSP Foods LLC — WFSP Foods, LLC Recalls Pork and Chicken Sausage Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V625000·2016-08-26

    Horton Ambulances Recalled for Air Conditioner Wiring Fire Risk

    Halcore Group is recalling 2013-2016 Horton ambulances because a poorly sealed air conditioner wire harness allows water entry, creating a risk of electrical fire.

    Product
    HORTON AMBULANCE — HORTON AMBULANCE 453, 457, CHANGE OVER, 623
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V624000·2016-08-26

    Midwest Fire Recalls 2016-2017 All-Poly Fire Trucks for Transmission Defect

    Midwest Fire is recalling 2016-2017 All-Poly 2500 and 3000 series fire trucks because a transmission component may fail, preventing the vehicle from pumping water.

    Product
    MIDWEST — MIDWEST ALL-POLY 3000 SERIES, ALL-POLY 2500 SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V623000·2016-08-26

    Tiffin Allegro Recall: Driver-Side Wiper Arm May Break

    Tiffin is recalling 2017 Allegro Open Roads because the driver-side wiper arm may break, reducing visibility and increasing crash risk.

    Product
    TIFFIN — TIFFIN ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V621000·2016-08-25

    Ford Recalls 2013-2015 Taurus, Flex, MKS, MKT for Fuel Pump Defect

    Ford is recalling 2013-2015 Taurus, Flex, MKS, and MKT vehicles because a fuel pump component may overheat, causing the engine to stall or preventing the vehicle from starting.

    Product
    LINCOLN — LINCOLN, FORD MKS, FLEX, MKT, TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16253·2016-08-25

    Whirlpool Recalls Microwave Hood Combinations Due to Fire Hazard

    Whirlpool is recalling about 15,200 microwave hood combinations because internal arcing can ignite plastic components, posing a fire hazard.

    Product
    Whirlpool brand microwave hood combinations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16251·2016-08-25

    M&M's Branded Jewelry Recalled for Lead Content Violations

    Mars Retail Group is recalling M&M's-branded jewelry due to high lead levels. Consumers should stop using the items and return them for a refund.

    Product
    M&M'S®-branded jewelry
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V622000·2016-08-25

    Bison Recalls 2015-2016 Horse Trailers Due to Missing Battery Fuse

    Bison Coach is recalling 654 model year 2015-2016 horse trailers because a missing inline fuse on the battery cable could cause overheating and fire during an electrical short.

    Product
    BISON — BISON RANGER, SILVERADO, TRAIL BOSS, TRAIL HAND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16252·2016-08-25

    Cree Recalls LED T8 Lamps Due to Overheating and Burn Hazard

    Cree is recalling LED T8 replacement lamps that can overheat and melt, posing a burn hazard. No injuries have been reported.

    Product
    Cree® LED T8 Replacement Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V620000·2016-08-25

    Seagrave Recalls Marauder II Fire Trucks Due to Transmission Defect

    Seagrave is recalling 28 Marauder II fire trucks because a transmission component may fail, preventing the vehicle from pumping water at fire scenes.

    Product
    SEAGRAVE — SEAGRAVE MARAUDER II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2533-2016·2016-08-24

    Baxter Recalls VASCU-GUARD Patches Due to Bleeding Reports

    Baxter Healthcare is recalling VASCU-GUARD Peripheral Vascular Patches due to postmarketing reports of intraoperative and postoperative bleeding, including one fatal outcome.

    Product
    Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and product codes: 1 cm x 6 cm, product code VG0106N, 0.8 cm x 8 cm, product code VG0108N, 1 cm x 10 cm, product code VG0110N, and 2 cm x 9 cm, product code VG0209N. VASC U-GUARD is prepared from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1933-2016·2016-08-24

    HelloFresh Recalls Lemony Pan-Seared Chicken Meal Due to Listeria Risk

    HelloFresh is recalling Lemony Pan-Seared Chicken with Pesto Potato Salad and Peas due to possible Listeria monocytogenes contamination.

    Product
    Lemony Pan-Seared Chicken with Pesto Potato Salad and Peas
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1935-2016·2016-08-24

    HelloFresh Recalls Lamb-Stuffed Zucchini Due to Listeria Risk

    HelloFresh is recalling 1,258 pounds of Nir's Lamb-Stuffed Zucchini with Spiced Lentil Stew due to possible Listeria monocytogenes contamination.

    Product
    Nir's Lamb-Stuffed Zucchini with Spiced Lentil Stew
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1934-2016·2016-08-24

    HelloFresh Recalls Seared Steak Meal Due to Listeria Risk

    HelloFresh is recalling Seared Steak with Spring Veggie Succotash and Mint-Chive Pesto due to possible Listeria monocytogenes contamination.

    Product
    Seared Steak with Spring Veggie Succotash and Mint-Chive Pesto
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Drugs)·D-1458-2016·2016-08-24

    Golden State Medical Supply Recalls Venlafaxine Hydrochloride Extended-Release Capsules

    Golden State Medical Supply Inc. is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, due to failed dissolution specifications.

    Product
    Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b) 90 capsules per bottle, NDC # 60429-123-90, Rx Only, GSMS.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2567-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recalled for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Flat L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 119,770 units distributed worldwide.

    Product
    Valleylab Laparoscopic Flat L-Hook Electrode 36CM Item Code: E277436 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction via a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1922-2016·2016-08-24

    Newly Weds Foods Recalls Flour Breader Contaminated with E. coli O121

    Newly Weds Foods Inc is recalling bulk flour bland breader contaminated with E. coli O121. The product was distributed nationwide in 15, 30, and 50 lb bags or boxes.

    Product
    Bulk flour bland breader packaged into 15, 30, and 50 lb bags or boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2575-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recall for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Wire L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 50,055 units distributed worldwide.

    Product
    Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code: E2783R36ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1932-2016·2016-08-24

    HelloFresh Recalls Summer Vegetable Salad Due to Listeria Risk

    HelloFresh is recalling Summer Vegetable Salad with Seared Chicken due to possible Listeria monocytogenes contamination. The product was distributed in 28 states.

    Product
    Summer Vegetable Salad with Seared Chicken, Garlic Croutons, and Mustard-Chive Vinaigrette
    Category
    Food
    Distribution
    28 states
  • HighFDA (Devices)·Z-2577-2016·2016-08-24

    Medtronic Recalls Laparoscopic Electrode Due to Sterile Barrier Compromise Risk

    Medtronic is recalling 3,470 Valleylab Laparoscopic Flat L-Hook Electrodes because the package may be compromised, potentially breaching the sterile barrier.

    Product
    Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code: E2784R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction…
    Category
    Medical Device
    Distribution
    Distributed nationwide