The Recall Desk

State

Nebraska product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44226–44250 of 78389

  • HighNHTSA·17V522000·2017-08-24

    Thor Motor Coach Recalls 2018 RVs for Propane Hose Leak Risk

    Thor Motor Coach is recalling 2018 Four Winds, Chateau, and Freedom Elite recreational vehicles because a liquid propane hose may sag and pinch, potentially causing a leak and fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, CHATEAU, FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17211·2017-08-24

    Dr. Martens Vegan Boots Recalled for Benzidine Chemical Exposure Hazard

    Airwair is recalling Dr. Martens Vegan 1460 boots in cherry red because the tongue lining contains benzidine. Consumers should stop using the boots and contact Dr. Martens for a refund or replacement.

    Product
    Dr. Martens Vegan boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1092-2017·2017-08-23

    GEC LX Laxoplex Recalled for Undeclared Anabolic Steroids

    Genetic Edge Compounds LLC is recalling GEC LX Laxoplex dietary supplements because FDA analysis found the product tainted with undeclared anabolic steroids and steroid-like substances.

    Product
    GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC: 700580499842
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1087-2017·2017-08-23

    Biotech Underground Tri-Ton Hardcore Formula Recalled for Unapproved Ingredients

    Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.

    Product
    Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations 12850 Hwy 9 Suite 600-441 Alpharetta, GA 30004
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3367-2017·2017-08-23

    NatureAll Acidophilus-Plus Recalled for Undeclared Milk Allergens

    NatureAll is recalling Acidophilus-Plus dietary supplements because they contain undeclared milk allergens, including colostrum, dried yogurt, and whey.

    Product
    Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3038-2017·2017-08-23

    Boston Scientific Recalls Emblem MRI S-ICD Devices Due to Energy Delivery Risk

    Boston Scientific is recalling approximately 9,200 Emblem MRI S-ICD devices because memory corruption may cause the device to deliver an atypical amount of energy.

    Product
    EMBLEM MRI S-ICD Model 219, Subcutaneous-Implantable Cardioverter Defibrillator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1085-2017·2017-08-23

    Hardcore Formulations Recalls D-ZINE Rapid Size and Strength Capsules

    Hardcore Formulations is recalling D-ZINE Rapid Size and Strength capsules because they contain unapproved active ingredients.

    Product
    D-ZINE Rapid Size and Strength capsules, 10mgs, 90 count bottle, Hardcore Formulations, UPC: 7 48252 86193 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3034-2017·2017-08-23

    Cenorin ThermaSure Medical Device Dryers Recalled for Overheating Terminal Block

    Cenorin, LLC is recalling 18 ThermaSure Series 1000 medical device dryers because a manufacturing defect causes the terminal block to overheat, char, or burn.

    Product
    ThermaSure(TM), a CENORIN(TM) product, SERIES 1000 MEDICAL DEVICE DRYER: (a) Model 1009; (b) Model 1010 Forced air dryer for medical devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1084-2017·2017-08-23

    FDA Recalls Ultra-Sten Capsules Marketed Without Approval

    Hardcore Formulations is recalling Ultra-Sten capsules because they contain unapproved ingredients and were marketed without an approved NDA or ANDA.

    Product
    ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1091-2017·2017-08-23

    ICU Medical Recalls 0.9% Sodium Chloride Injection Due to Particulate Matter

    ICU Medical Inc. is recalling 436,716 units of 0.9% Sodium Chloride Injection due to the presence of stainless steel particulate matter.

    Product
    0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3039-2017·2017-08-23

    Boston Scientific Recalls SQ-RX 1010 Pulse Generators Due to Memory Corruption

    Boston Scientific is recalling approximately 12,450 SQ-RX 1010 Pulse Generators because memory corruption may cause the device to deliver an atypical amount of energy.

    Product
    SQ-RX 1010 Pulse Generator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic bradycardia, incessant ventricular tachycardia, or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3037-2017·2017-08-23

    Boston Scientific Recalls Emblem S-ICD Devices Due to Energy Delivery Risk

    Boston Scientific is recalling approximately 16,750 Emblem S-ICD devices because they may deliver atypical energy levels due to internal memory corruption.

    Product
    EMBLEM S-ICD, Model A209, Subcutaneous Implantable Cardioverter Defibrillator, RX. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1093-2017·2017-08-23

    Lupin Recalls Mibelas 24 Fe Contraceptive Tablets Due to Sequence Error

    Lupin Limited is recalling Mibelas 24 Fe tablets because the first four pills in the packet are brown instead of the last four, and the expiry/lot was not printed on the package.

    Product
    Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02 mg chewable and ferrous Fumarate 75 mg) Tablets, wallet of 28 tablets (NDC 68180-911-11), Carton of 3 wallets (NDC 68180-911-13), Rx Only, Manufactured by: Lupin Limited, India, Distributed by Lupin…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17209·2017-08-23

    Nutrilife Recalls 29% Hydrogen Peroxide Bottles Due to Fire and Burn Hazards

    Nutrilife is recalling 29% hydrogen peroxide bottles because caps may not vent properly, allowing pressure to build and cause rupture, posing fire and burn risks.

    Product
    Nutrilife 29% hydrogen peroxide (H202) one-gallon bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3368-2017·2017-08-23

    FDA Recalls Metabo-Plus Dietary Supplement for Undeclared Milk Allergen

    NatureAll-STF Holding, LLC is recalling 254 bottles of Metabo-Plus dietary supplement because it contains undeclared milk (whey), a major allergen.

    Product
    Metabo-Plus, Garlic/Papaya Plus, No. 103, 90 Capsules, Dietary Supplement
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3366-2017·2017-08-23

    Aldi Gluten Free Hamburger Buns Recalled for Undeclared Eggs

    Silver Hills Bakery is recalling Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns due to undeclared eggs. The recall affects 9,639 retail units sold nationwide.

    Product
    Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns, 11.3 Ounces, in plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3369-2017·2017-08-23

    NatureAll Thymus Plus Recalled for Undeclared Milk Allergen

    NatureAll is recalling Thymus Plus dietary supplements because they contain undeclared milk. Consumers with milk allergies should not use the product.

    Product
    Thymus Plus, No. 114, 90 Capsules, Dietary Supplement
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2720-2017·2017-08-23

    High Liner Breaded Fish Recalled for Undeclared Milk Allergen

    High Liner Foods is recalling Oven Ready Whole Grain Breaded Fish Sea Wonders due to potential undeclared milk. Consumers with milk allergies should not consume the product.

    Product
    HFS 1/10 Oven Ready Whole Grain Breaded Fish Sea Wonders, Item Number: 26533
    Category
    Food
    Distribution
    Distributed nationwide