The Recall Desk

State

Nebraska product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59376–59400 of 78413

  • SevereNHTSA·15V020000·2015-01-20

    Polaris Recalls 2015 Slingshot Motorcycles Due to Roll Hoop Defect

    Polaris is recalling 2015 Slingshot and Slingshot SL motorcycles because roll hoops may not meet hardness specifications, increasing injury risk in rollovers.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V017000·2015-01-20

    Jayco Eagle Fifth Wheel Trailers Recalled for Incorrect Tire Labeling

    Jayco is recalling 2015 Eagle 30.5 BHLT fifth wheel trailers because the tire labels list incorrect tire sizes. Owners should contact Jayco to receive corrected labels to prevent potential tire failure.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V019000·2015-01-20

    Volkswagen Recalls Audi and VW Models for Fuel Leak Fire Risk

    Volkswagen is recalling 26,008 Audi and Volkswagen vehicles because a fuel leak in the injection system could cause a fire.

    Product
    AUDI — AUDI, VOLKSWAGEN A7, A6, TOUAREG HYBRID, S4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V018000·2015-01-20

    Frontline Mobile Medical Units Recalled for Wheelchair Lift Defect

    Frontline Communications is recalling 2007-2011 Mobile Medical Units because wheelchair lift platform side plates may crack, posing an injury risk.

    Product
    FRONTLINE COMMUNICATIONS — FRONTLINE COMMUNICATIONS MOBILE MEDICAL UNIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E001000·2015-01-20

    Tucker Rocky Recalls Speed and Strength SS500DVD Motorcycle Helmets

    Tucker Rocky is recalling specific Speed and Strength SS500DVD motorcycle helmets because they fail to meet federal safety standards, increasing the risk of serious injury in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·014-2015·2015-01-17

    La Guadalupana Recalls Chicken Tamales Lacking Required Safety Plans

    La Guadalupana Wholesale is recalling chicken tamales produced without required HACCP and Listeria programs. No illnesses have been reported.

    Product
    La Guadalupana — Illinois Firm Recalls Chicken Products Produced Without Adequate Ready-To-Eat HACCP Plan and a Listeria Monocytogenes Program
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·016-2015·2015-01-17

    Sentry Food Solutions Recalls Chicken and Beef Products for Undeclared Peanuts

    Sentry Food Solutions is recalling approximately 14,130 pounds of chicken and beef products because they may contain undeclared peanuts.

    Product
    Georgia Firm Recalls Chicken and Beef Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·015-2015·2015-01-17

    Kalle USA Recalls Pork Products Produced Without Inspection

    Kalle USA is recalling approximately 168,473 pounds of dehydrated pork products that were not presented for U.S. inspection. No adverse reactions have been reported.

    Product
    Illinois Firm Recalls Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·014-2015(Original)·2015-01-17

    La Guadalupana Recalls Chicken Tamales Lacking Required Safety Plans

    La Guadalupana Wholesale is recalling 8,856 pounds of chicken tamales because they were produced without a required HACCP plan or Listeria program.

    Product
    La Guadalupana — Illinois Firm Recalls Chicken Products Produced Without Adequate Ready-To-Eat HACCP Plan and a Listeria Monocytogenes Program
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0905-2015·2015-01-14

    DePuy ATTUNE INTUITION Impactors Recalled Due to Fracture Risk

    DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they have broken and produced small pieces that could be left in patients during knee replacement surgery.

    Product
    Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home its…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2015·2015-01-14

    Agri Star Recalls Beef Franks for Undeclared Peanuts and Misbranding

    Agri Star Meat & Poultry is recalling 1,690 pounds of beef franks that may contain undeclared peanuts and are misbranded as gluten-free.

    Product
    Agri Star Meat and Poultry, LLC — Iowa Firm Recalls Beef Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0880-2015·2015-01-14

    Alere INRatio PT/INR Test Strips Recalled for Inaccurate Results

    Alere San Diego, Inc. is recalling INRatio PT/INR Test Strips because the system may provide INR results significantly lower than reference laboratory methods.

    Product
    Alere INRatio PT/INR Test Strips, Alere INRatio PT/INR System Professional - 0100071 Alere INRatio PT/INR Test Strips, Box of 12 - 0100139 Alere INRatio PT/INR Test Strips, Box of 48 The test strips are packaged in individually pouched test strips in a labeled box with 12…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0903-2015·2015-01-14

    DePuy ATTUNE INTUITION Impactors Recalled for Fracture Risk During Surgery

    DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they have broken and produced small pieces that could be left in patients during knee replacement surgery.

    Product
    Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home its…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0904-2015·2015-01-14

    DePuy ATTUNE INTUITION Impactors Recalled Due to Fracture Risk

    DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they may break during knee surgery, potentially leaving small fragments in the patient.

    Product
    Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0881-2015·2015-01-14

    Alere INRatio Monitors Recalled for Potential Inaccurate INR Results

    Alere San Diego, Inc. is recalling INRatio PT/INR Monitor systems because they may provide INR results significantly lower than reference laboratory methods.

    Product
    INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional - 0100007 INRatio Prothrombin Time (PT) Monitoring System - 0100137 Alere INRatio Replacement Monitor The test systems contain individually packaged components needed to use the product, such as a monitor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0334-2015·2015-01-14

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Sterility Concerns

    Hospira Inc. is recalling 30,840 bags of 0.9% Sodium Chloride Injection, USP, 100mL, due to a potential leak at the administrative port that compromises sterility.

    Product
    0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0882-2015·2015-01-14

    Alere INRatio 2 Monitors Recalled for Potential Inaccurate INR Results

    Alere San Diego, Inc. is recalling INRatio 2 PT/INR monitors because they may provide results significantly lower than reference laboratory methods.

    Product
    INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Testing System - 0200432 Alere INRatio 2 PT/INR Home Monitoring System - 0200433 Alere INRatio 2 PT/INR Home Monitoring System - 0200457 Alere INRatio 2 Replacement Monitor - 55112 Alere INRatio 2 Replacement…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V010000·2015-01-14

    Winnebago Recalls 2013-2015 Travel Trailers Due to Propane Leak Risk

    Winnebago is recalling specific 2013-2015 Minnie and Sunnybrook Remington travel trailers because the axle may crack the propane pipe fitting, creating a fire hazard.

    Product
    WINNEBAGO — WINNEBAGO, SUNNYBROOK MINNIE, REMINGTON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0908-2015·2015-01-14

    DePuy I.M. Hole Locator Instrument Recalled for Fracture Risk

    DePuy Orthopaedics is recalling 1,130 I.M. Hole Locator Instruments because excessive force during use may lead to intra-operative femoral fracture.

    Product
    I.M. Hole Locator Instrument. Orthopedic manual surgical instrument. The IM Hole locator guides the IM drill during IM Hole preparation. The instrument is positioned between the condyles and aligned with the anatomical axis. Pins can be placed in the IM hole locator to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0931-2015·2015-01-14

    Synthes Small Electric Drive Recalled for Unintended Start and Malfunction

    Synthes (USA) Products LLC is recalling 12 Small Electric Drive units due to potential unintended starts or reverse mode failures that could cause tissue damage.

    Product
    Synthes Small Electric Drive (SED), part number: 05.001.175: The Small Electric Drive is designed for use in general traumatology, especially hand and food applications involving surgical procedures such as drilling, burring, reaming, pin and wire placement, cutting of bone and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0764-2015·2015-01-14

    Abdallah Caramel Bites Recalled for Peanut Contamination

    Abdallah Candies is recalling Holiday Caramel Bites because a customer found a peanut butter bite in the package.

    Product
    Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate (sugar, chocolate liquor, cocoa butter, whole milk, soy lecithin (an emulsifier), vanilla), corn syrup, sweetened condensed milk, cream, sugar, palm oil, salt…
    Category
    Food
    Distribution
    35 states