The Recall Desk

State

Nebraska product recalls

73,566 recalls have nationwide distribution and so reach Nebraska. 4,576 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,576
Critical
715
Severe
1,343
Most recent
2026-10-14

Of the 4,576 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,343 (29%) are Severe.

Which agencies issued them

These figures cover only the 4,576 recalls whose distribution notice names Nebraska specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25626–25650 of 78142

  • HighCPSC·21770·2021-07-29

    Specialized Electric Mountain Bike Battery Packs Recalled for Fire and Burn Hazards

    Specialized is recalling about 2,500 first-generation Turbo Levo and Kenevo electric mountain bike battery packs because water can penetrate the seal around the LED control pad and cause the battery to short circuit, creating fire and burn hazards.

    Product
    Specialized 1st Generation Turbo Levo and Kenevo electric mountain bike battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V583000·2021-07-29

    NRC Recalls 2019-2020 Motorhomes Due to Gas Leak Risk

    NRC is recalling 2019-2020 motorhomes because an overtightened stove bolt may damage the seal, causing a gas leak that increases fire risk.

    Product
    NRC — NRC MOTOR HOME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V578000·2021-07-29

    2020-2021 Silverado 2500 and Sierra 2500 Spare Tire ABS Failure Recall

    General Motors is recalling 2020-2021 Silverado 2500 and Sierra 2500 trucks where a 17-inch spare tire paired with larger road tires prevents ABS from engaging, raising crash risk. Dealers will replace the spare tire and label at no cost.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 2500, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V584000·2021-07-29

    Land Rover Defender Recall for Incorrect Child Seat Manual Information

    Jaguar Land Rover is recalling 2020-2021 Defender vehicles because the owner's manual incorrectly states that third-row seats have LATCH top tethers, which may lead to improper child seat installation.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21769·2021-07-29

    Children's Sleepwear Sets Recalled for Flammability Standard Violation

    SHEIN children's sleepwear sets fail to meet federal flammability standards and pose a burn injury risk. About 2,320 units sold online from August 2019 through January 2021 are affected.

    Product
    Children's Sleepwear Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V589000·2021-07-29

    Spartan RV Chassis Instrument Cluster May Intermittently Go Blank

    Shyft Group is recalling certain 2018-2022 Spartan RV Chassis models (K1, K2, K3, K4) because the instrument cluster may intermittently go blank while the vehicle is in motion, potentially obscuring critical speed and warning information.

    Product
    SPARTAN — SPARTAN K2, K4, K3, K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0685-2021·2021-07-28

    Shogun-X 7000 Capsules Recalled for Undeclared Prescription Drug Ingredients

    Nuri Trading LLC is recalling Shogun-X 7000 capsules nationwide because they contain undeclared tadalafil and sildenafil, FDA-approved prescription drugs not listed on the label, making the product an unapproved drug.

    Product
    Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0686-2021·2021-07-28

    Thumbs Up 7 Black 25K Capsules Recalled for Undeclared Tadalafil

    Nuri Trading LLC is recalling Thumbs Up 7 Black 25K capsules nationwide because they contain undeclared tadalafil, an FDA-approved drug. The product was marketed without required approval, making it an unapproved drug with unestablished safety and efficacy.

    Product
    Thumbs Up 7 Black 25K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0682-2021·2021-07-28

    Goose Creek Hand Sanitizer Recalled for Chemical Contamination

    Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer Aloe Watermelon Lemonade due to contamination with methanol, benzene, and acetaldehyde. The 3.38 FL. OZ. bottles were distributed nationwide.

    Product
    Goose Creek Hand Sanitizer aloe Watermelon Lemonade, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 814630 02423 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0677-2021·2021-07-28

    Goose Creek Hand Sanitizer Recalled for Methanol and Chemical Contamination

    Goose Creek Hand Sanitizer aloe Dragonfruit Splash (3.38 FL. OZ.) is being recalled because the product is contaminated with methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.

    Product
    Goose Creek Hand Sanitizer aloe Dragonfruit Splash, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 18489 01332 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0663-2021·2021-07-28

    Shogun-X Capsules Recalled for Undeclared Prescription Drug Ingredients

    Shogun-X capsules have been recalled because they contain undeclared tadalafil, sildenafil, and/or vardenafil—prescription drugs not listed on the label. These are unapproved drugs whose safety and efficacy have not been established.

    Product
    Shogun-X capsules, 10-count boxes, Manufactured by Power Life Distributors, Made in USA, UPC 118122030185
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0679-2021·2021-07-28

    Goose Creek Hand Sanitizer Recalled for Methanol and Benzene Contamination

    Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer aloe Melon Picnic spray (3.38 FL. OZ., Lot #20259) due to contamination with methanol, benzene, and acetaldehyde.

    Product
    Goose Creek Hand Sanitizer aloe Melon Picnic, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 14630 02424 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0671-2021·2021-07-28

    SS Tangerine & Guava Scented Sanitizer Recalled for Chemical Contamination

    Scentsational Soaps & Candles Inc is recalling SS Tangerine & Guava Scented Sanitizer (3.38 FL. OZ.) due to contamination with methanol, benzene, and acetaldehyde. The product was distributed nationwide.

    Product
    SS Tangerine & Guava Scented Sanitizer, Alcohol Antiseptic 70%, Non-sterile Topical Solution, 3.38 FL. OZ. (100 mL) a) Black and White Collection; b) Photo Real Collection
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0662-2021·2021-07-28

    Krazy Night Capsules Contain Undeclared Prescription Drug Ingredients

    Krazy Night capsules (1-count blister cards and 10-count boxes) are being recalled nationwide because they contain undeclared tadalafil, sildenafil, and/or vardenafil without FDA approval. These unapproved drugs have not undergone safety and efficacy review.

    Product
    Krazy Night capsule, packaged in a) 1-count per blister card and b) 10-count boxes, Manufactured by: SUM MARKETING LLC, Made in USA UPC 746695241860
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0692-2021·2021-07-28

    Compounded Semorelin/Ipamorelin Injection Recalled for Sterility Assurance

    Innoveix Pharmaceuticals is recalling 728 vials of compounded Semorelin/Ipamorelin 3 mg injection due to lack of assurance of sterility. The affected lots are SIP215, SIP220, and SIP210.

    Product
    Compounded Lyophilized Semorelin/Ipamorelin 3 mg For subcutaneous or intramuscular injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0668-2021·2021-07-28

    SS Eucalyptus Mint Scented Sanitizer Recalled for Chemical Contamination

    Scentsational Soaps & Candles Inc is recalling SS Eucalyptus Mint Scented Sanitizer due to contamination with methanol, benzene, and acetaldehyde. The affected product was distributed nationwide.

    Product
    SS Eucalyptus Mint Scented Sanitizer, Alcohol Antiseptic 70%, Non-sterile Topical Solution, 3.38 FL. OZ. (100 mL), a) Black and White Collection; b) Photo Real Collection
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0794-2021·2021-07-28

    MCT Powder 70% from Coconut Recalled for Milk Allergen

    Nutralliance Inc is recalling Medium Chain Triglyceride (MCT) Powder 70% from Coconut distributed in bulk to supplement manufacturers because an ingredient tested positive for milk allergen.

    Product
    Medium Chain Triglyceride (MCT) Powder 70% from Coconut / CocoTrim packaged in 20 kilogram brown bags with plastic inner lining for bulk sale to supplement manufacturers. Exclusively Distributed by Nutralliance / Manufactured by Bio-gen Extracts Pvt. Ltd. Store tightly sealed…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2074-2021·2021-07-28

    Philips Respironics V60 Plus Ventilator software defect reduces oxygen delivery to patients

    Respironics V60 Plus Ventilators (software versions 3.00 and 3.10) may reduce oxygen flow below clinical settings, risking oxygen desaturation and hypoxemia in mechanically ventilated patients.

    Product
    Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an assist ventilator and is intended to augment patient breathing. It is intended for spontaneously breathing individuals who require mechanical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0684-2021·2021-07-28

    Coconut Stand CoCo TKO Hand Sanitizer Contaminated with Methanol, Benzene, Acetaldehyde

    Scentsational Soaps & Candles Inc is recalling Coconut Stand CoCo TKO Hand Sanitizer due to contamination with methanol, benzene, and acetaldehyde. The product was distributed nationwide in 3.4 FL. OZ. bottles.

    Product
    Coconut Stand CoCo TKO Hand Sanitizer, Totally Knocks Out 99.9% of Germs, 3.4 FL. OZ. (100.55 mL), Distributed by: Beauty Sparks LLC St. Petersburg, FL 33711
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0675-2021·2021-07-28

    Goose Creek Hand Sanitizer Spray Recalled for Chemical Contamination

    Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer aloe Grape Soda spray because it contains methanol, benzene, and acetaldehyde. The contaminated product was distributed nationwide.

    Product
    Goose Creek Hand Sanitizer aloe Grape Soda, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 18489 01328 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V576000·2021-07-28

    New Flyer Recalls 2021 XD35 and XD40 Buses for Fuel Leak Risk

    New Flyer is recalling 2021 XD35 and XD40 buses with Cummins L9 engines due to a potential fuel hose leak that could cause a fire.

    Product
    NEW FLYER — NEW FLYER XD35, XD40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0676-2021·2021-07-28

    Goose Creek Hand Sanitizer Spray Recalled for Chemical Contamination

    Goose Creek Hand Sanitizer aloe Champagne Bubbles spray (3.38 FL. OZ.) has been recalled because it is contaminated with methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.

    Product
    Goose Creek Hand Sanitizer aloe Champagne Bubbles, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 18489 01334 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0667-2021·2021-07-28

    SS Coconut Breeze Scented Sanitizer Recalled for Chemical Contamination

    SS Coconut Breeze Scented Sanitizer has been recalled due to contamination with methanol, benzene, and acetaldehyde. The 3.38 FL. OZ. bottles were distributed nationwide.

    Product
    SS Coconut Breeze Scented Sanitizer, Alcohol Antiseptic 70%, Non-sterile Topical Solution, 3.38 FL. OZ. (100 mL), a) Black and White Collection; b) Photo Real Collection
    Category
    Drug
    Distribution
    Distributed nationwide