The Recall Desk

State

Nebraska product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55951–55975 of 78407

  • SevereNHTSA·15V562000·2015-09-04

    New Flyer Transit Buses Recalled for Potential Steering Loss

    New Flyer is recalling 432 transit buses from 2013-2015 because a tie rod clamp may be improperly torqued, risking a loss of steering.

    Product
    NEW FLYER — NEW FLYER XN40, XN35, XD40, XD60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V561000·2015-09-04

    Keystone Recalls 2008-2009 Travel Trailers Due to Fire Risk

    Keystone is recalling 2008-2009 travel trailers and fifth wheels because a transfer switch may overheat and cause a fire.

    Product
    KEYSTONE — KEYSTONE CHALLENGER, RAPTOR, BIG SKY, EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V564000·2015-09-04

    Thomas Built Buses Recall Wheelchair Lifts Due to Bearing Defect

    Daimler Trucks North America is recalling 2006-2015 Thomas Built Buses equipped with certain Ricon wheelchair lifts. Defective pivot holes may allow bearings to move, risking platform failure and injury.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER EF, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V565000·2015-09-04

    Thomas Built Buses Recall Wheelchair Lifts with Potential Bearing Failure

    Daimler Trucks North America is recalling 4,334 Thomas Built Buses equipped with specific Ricon wheelchair lifts due to a defect that could cause the platform to fall.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EF, SAF-T-LINER FS65, SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V557000·2015-09-03

    Fontaine Recalls 2015 Traverse HT Trailers Due to Suspension Defect

    Fontaine Trailer Company is recalling 2015 Traverse HT trailers because a suspension member may separate from the trailer, increasing the risk of a crash.

    Product
    FONTAINE — FONTAINE TRAVERSE HT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15232·2015-09-03

    Prestone Windshield De-Icer and Ice & Frost Shield Recalled for Child Safety

    Prestone is recalling about 4.1 million bottles of windshield de-icer and frost shield because the trigger sprays can be removed, allowing children access to toxic chemicals.

    Product
    Prestone® Windshield De-Icer and Prestone® Ice & Frost Shield
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15231·2015-09-03

    Cannondale Mountain Bicycles Recalled for Stem Failure and Fall Risk

    Cycling Sports Group is recalling about 23,000 Cannondale mountain bicycles because the OPI stem/steering tube can fail, posing a risk of injury from a fall.

    Product
    Cannondale mountain bicycles with OPI stem/steering tube
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1351-2015·2015-09-02

    Teva Recalls ADRUCIL Fluorouracil Injection Due to Particulate Matter

    Teva Pharmaceuticals USA is recalling ADRUCIL (fluorouracil injection) vials due to the presence of silicone rubber and fluorouracil crystals in the solution.

    Product
    ADRUCIL (fluorouracil injection, USP), 5 g/100 mL (50 mg/mL) glass vials, 5 x 100 ml vials per carton, manufactured by Teva Parenteral Medicines, Inc., Irvine, CA. NDC 073-3019-11 (individual vial), NDC 0703-3019-12 (carton of five).
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3045-2015·2015-09-02

    Kroger Black Pepper Recalled Due to Salmonella Contamination

    Kroger is recalling Black Pepper Coarse Ground because a related product tested positive for Salmonella. The recall covers items produced on the same filling line.

    Product
    Kroger Black Pepper Coarse Ground UPC 11110 70041 NET WT 17.1 oz plastic container
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Drugs)·D-1357-2015·2015-09-02

    PharMEDium Recalls Heparin Sodium Injection Bags Due to Particulate Matter

    PharMEDium Services, LLC is recalling 240 bags of Heparin Sodium Injection USP 25,000 Units in 250 mL bags due to the presence of particulate matter.

    Product
    HEPARIN Sodium Injection USP 25,000 USP Units added to 250 mL 5% Dextrose Injection USP (100 units per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K0419, NDC# 61553-419-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1356-2015·2015-09-02

    PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter

    PharMEDium Services, LLC is recalling 48 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.

    Product
    EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Chloride Injection USP (64 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6618, NDC# 61553-618-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1358-2015·2015-09-02

    PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter

    PharMEDium Services, LLC is recalling 264 bags of Epinephrine HCl injection due to the presence of particulate matter in the saline solution.

    Product
    EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Chloride Injection USP (16 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6119, NDC# 61553-119-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3043-2015·2015-09-02

    Kroger Ground Cinnamon Recalled Due to Salmonella Risk on Filling Line

    The Kroger Co is recalling specific lots of Ground Cinnamon because a related product on the same line tested positive for Salmonella.

    Product
    Kroger Ground Cinnamon UPC 11110 70034 NEW WT. 18.3 oz Plastic container
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-3046-2015·2015-09-02

    Kroger Artificial Bacon Flavored Chips Recalled Due to Salmonella Risk

    The Kroger Co is recalling specific lots of Kroger Bac'n Buds Artificial Bacon Flavored Chips because a related product tested positive for Salmonella.

    Product
    Kroger Bac'n Buds ARTIFICIAL BACON FLAVORED CHIPS 14.1oz plastic container UPC 0 11110 70025 4
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Drugs)·D-1354-2015·2015-09-02

    PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter

    PharMEDium Services is recalling 36 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.

    Product
    EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Chloride Injection USP (4 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6244, NDC# 61553-244-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1365-2015·2015-09-02

    Mucinex Fast-Max Cold & Sinus Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast-Max Cold & Sinus liquid because the back of the bottle is missing active ingredients and safety warnings.

    Product
    Mucinex Fast-Max Cold & Sinus, Maximum Strength, Acetaminophen Pain Reliever/Fever Reducer, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Ages 12+, Dist. by: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1363-2015·2015-09-02

    Mucinex Fast-Max Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.

    Product
    MUCINEX FAST-MAX — MUCINEX FAST-MAX (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1366-2015·2015-09-02

    Mucinex Fast-Max Liquid Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.

    Product
    Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Time Cold & Flu Two - 6 fl oz (180 mL) bottles Total -12 fl oz (360 mL), For Age 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC 63824-526-22
    Category
    Drug
    Distribution
    Distributed nationwide