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.

57551–57575 of 78413

  • HighCPSC·15138·2015-05-19

    Precision Trading Recalls Espresso Makers Due to Burn Risk

    Precision Trading is recalling about 4,700 PREMIUM Espresso Makers because the filler cap can crack or pop off, releasing steam and posing a burn risk.

    Product
    PREMIUM® Espresso Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15139·2015-05-19

    Kaldi's Coffee Recalls Disposable Cup Sleeves Due to Fire Hazard

    Kaldi's Coffee Roasting is recalling about 700,000 disposable paper cup sleeves because they can ignite in microwaves. Two fire incidents were reported, with no injuries.

    Product
    Disposable Cup Sleeves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V295000·2015-05-19

    Gillig Low Floor Bus Taillight Bracket Recall

    Gillig is recalling 2014-2015 Low Floor buses because taillight brackets may detach, reducing visibility and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·15E040000·2015-05-18

    Takata Frontal Driver Air Bag Inflator Module Recall

    Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E042000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for Honda, Toyota, Pontiac, Subaru

    Takata is recalling PSPI-L passenger air bag inflators in specific Honda, Toyota, Pontiac, and Subaru models. The inflators may rupture in a crash, sending metal fragments into the vehicle.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V290000·2015-05-18

    RAM 4500 and 5500 Trucks Recalled for Tire Speed Rating Mismatch

    Chrysler is recalling 2014-2015 RAM 4500 and 5500 trucks because their tires are rated for a lower speed than the vehicle's maximum capability, posing a crash risk.

    Product
    RAM — RAM 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E041000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for 2001-2008 Vehicles

    Takata is recalling specific passenger frontal air bag inflators for 2001-2008 vehicles due to a risk of rupture during deployment.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V292000·2015-05-18

    New Flyer Buses Recalled for Engine Vent Tube Fire Risk

    New Flyer is recalling certain 2008-2014 buses because a vent tube may detach, allowing engine oil to contact hot surfaces and increase fire risk.

    Product
    NEW FLYER — NEW FLYER C40LF, C40LFR, C35LF, C35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V291000·2015-05-18

    Fiat 500 Electric Recall for Transmission Shifting to Neutral

    Chrysler is recalling 2013-2015 Fiat 500 electric vehicles because a software issue may cause the transmission to unexpectedly shift to neutral, increasing crash risk.

    Product
    FIAT — FIAT 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V288000·2015-05-15

    Daimler Orion VII Buses Recalled for Engine Fire Risk

    Daimler Buses North America is recalling 2007-2012 Orion VII natural gas buses because engine oil may contact hot surfaces, increasing fire risk.

    Product
    ORION — ORION VII
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V287000·2015-05-15

    Nissan Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk

    Nissan is recalling specific 2001-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the vehicle.

    Product
    NISSAN — NISSAN, INFINITI PATHFINDER, FX35, I30, FX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E039000·2015-05-15

    Industrial Axle Company Recalls ALKO AXIS Trailer Axle Hubs

    Industrial Axle Company is recalling specific ALKO AXIS trailer axles because wheel mounting studs may fail, potentially causing wheel separation and increasing crash risk.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·079-2015·2015-05-14

    AA Poultry Recalls Chicken and Turkey Due to Unapproved Substance

    AA Poultry Processing is recalling chicken and turkey products contaminated with trichloro-s-triazinetrione, an unapproved substance.

    Product
    Pine Creek Processing LLC — AA Poultry Processing, LLC Recalls Chicken and Turkey Products Due to Use of Unapproved Substance
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0977-2015·2015-05-13

    FDA Recalls EDGE Weight Release Capsules Containing Unapproved Drugs

    Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.

    Product
    EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00417 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0991-2015·2015-05-13

    Ultra ZX Dietary Supplement Recalled for Undeclared Sibutramine and Phenolphthalein

    Ultra ZX Labs is recalling Ultra ZX dietary supplements because FDA testing found undeclared sibutramine and phenolphthalein. The product was marketed without an approved NDA or ANDA.

    Product
    ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70, Extracto de semilla de Sen 47.6, Lagrima de Coix 42, Almidon Medico 84), 30 capsule bottles, Manufactured and distributed by: Ultra ZX Labs, L.L.C. 2525 SW 3rd Ave Apt 1704 Miami, Florida 33129-2068.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0981-2015·2015-05-13

    FDA Recalls iNSANE Bee Pollen Capsules Containing Unapproved Drugs

    The FDA is recalling iNSANE Bee Pollen capsules because they contain undeclared phenolphthalein and fluoxetine, making them unapproved drugs.

    Product
    iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00408 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0994-2015·2015-05-13

    Forever Beautiful Bee Pollen Recalled for Contaminants

    REFA Enterprises is recalling Forever Beautiful Bee Pollen capsules because FDA analysis found the product contains sibutramine and phenolphthalein.

    Product
    Forever Beautiful BEE POLLEN, capsules, 250mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0993-2015·2015-05-13

    REFA Enterprises Recalls Forever Beautiful INFINITY Capsules for Unapproved Ingredients

    REFA Enterprises is recalling Forever Beautiful INFINITY capsules because FDA analysis found the product contains sibutramine and phenolphthalein without an approved NDA/ANDA.

    Product
    Forever Beautiful INFINITY, capsules, 300mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0988-2015·2015-05-13

    FDA Recalls Estrastain Pro-Anabolic Mass and Hardening Complex Capsules

    Anabolic Science Labs LLC is recalling Estrastain Pro-Anabolic Mass and Hardening Complex capsules because they contain unapproved synthetic hormone ingredients.

    Product
    ESTRASTAIN PRO-ANABOLIC MASS AND HARDENING COMPLEX (Estra-4,9,11-triene-3,17-dione 15mg, 2a-3a-epithio-17a-methyl-5a-androstan-17b-ol 10 mg), Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0989-2015·2015-05-13

    FDA Recalls Unapproved Anabolic Steroid Supplements from Anabolic Science Labs

    Anabolic Science Labs is recalling SWOLL-250 Super Mass Builder Quad Stack capsules because they contain unapproved synthetic hormone ingredients.

    Product
    SWOLL-250 SUPER MASS BUILDER QUAD STACK (18-Methylestr-4-en-3-one-17b-ol 15mg, 6-a-Chloro-androst-4-en-17b-ol-3-one 15mg, 13-ethyl-3-methoxy-gona-2,5(10)-diene-17-one 15mg, 2,17a-dimethyl-5a-androsta-1-en-17b-ol-3-one 3 mg), Capsules, 90 count bottle, Manufactured for: Wyked…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2153-2015·2015-05-13

    Spiceco Recalls Hungarian Paprika Due to Undeclared Peanut Protein

    Spiceco is recalling Pride of Szeged Sweet Hungarian Paprika because it may contain undeclared peanut protein. The recall includes additional products containing the implicated paprika.

    Product
    Pride of Szeged Hungarian Exquisite 100 % Sweet Delicacy Paprika, Net Wt. 5 oz., 142g, UPC 0 78006 00010 2
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0979-2015·2015-05-13

    AMPD GOLD Bee Pollen Recalled for Undeclared Sildenafil

    Detox Transforms is recalling AMPD GOLD Bee Pollen capsules because they contain undeclared sildenafil, making them unapproved drugs.

    Product
    AMPD GOLD Bee Pollen capsules, 350 mg, 60-count bottle, Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00418 1.
    Category
    Drug
    Distribution
    Distributed nationwide