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.

58426–58450 of 78413

  • ModerateFDA (Devices)·Z-1408-2015·2015-04-15

    VasoNova Vascular Positioning System G4 Console Recalled for Standard Noncompliance

    VasoNova is recalling 17 Vascular Positioning System G4 Consoles due to noncompliance with IEC Standard 60101-1-1.

    Product
    VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number VPS-G4C Cardiovascular: The VPS Stylet and Console are indicated for guidance and tip positioning for central venous catheters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1396-2015·2015-04-15

    Bacterin OsteoSponge Instrument Kits Recalled for Sterilization Errors

    Bacterin International is recalling 63 Instrument Kits for OsteoSponge SC grafts because the instructions for use contain incorrect sterilization parameters.

    Product
    Instrument Kit for use with OsteoSponge SC grafts. The Instrument Kit is used to insert OsteoSponge SC grafts to fill bone defects in the subchondral region of articulating joints. The Instrument Kit is used to establish and maintain a port of entry for arthroscopic…
    Category
    Medical Device
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-1379-2015·2015-04-15

    TEM Systems Recalls ROTROL P Control Vials Due to Partial Filling

    TEM Systems Inc is recalling specific lots of ROTROL P Control vials because some were found to be partially filled.

    Product
    ROTROL P Control for ROTEM delta Thromboelastometry System, Manufactured for: Tem Innovations GmbH.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0436-2015·2015-04-15

    Heritage Pharmaceuticals Recalls Gliptizide and Metformin Tablets Due to Impurity

    Heritage Pharmaceuticals is recalling specific lots of Gliptizide and Metformin HCL tablets because they failed impurity specifications. The affected bottles were distributed nationwide.

    Product
    GLIPIZIDE AND METFORMIN HCL — GLIPIZIDE AND METFORMIN HCL (GLIPIZIDE AND METFORMIN HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0435-2015·2015-04-15

    Mylan Recalls Fexofenadine HCl Tablets Due to Impurity Failures

    Mylan Pharmaceuticals is recalling specific lots of Fexofenadine HCl 60 mg tablets because they failed impurity specifications. The recall covers 13,856 bottles distributed nationwide.

    Product
    Fexofenadine HCl Tablets, USP, 60 mg, Allergy, Antihistamine, Indoor and Outdoor Allergies, Non-Drowsy, Original Prescription Strength, a) 60 count Bottles, NDC 0378-0781-91, b) 500 count Bottles, NDC 0378-0781-05, Manufactured by: Mylan Pharmaceuticals Inc, Morgantown, WV…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D00432-2015·2015-04-15

    Qualitest Recalls Promethazine VC With Codeine Syrup Due to Impurity

    Qualitest Pharmaceuticals is recalling Promethazine VC with Codeine Syrup because a stability lot failed impurity specifications.

    Product
    PROMETHAZINE VC WITH CODEINE SYRUP, EACH 5 ml contains: Codeine Phosphate 10 mg, Promethazine Hydrochloride 6.25 mg, Phenylephrine Hydrochloride 5 mg, alcohol 7%, (a) 4 fl oz bottle (NDC 0603-1588-54) and (b) 16 fl oz bottle (NDC 0603-1588-58) Rx only, Manufactured for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V219000·2015-04-14

    Gillig Recalls 2013-2015 Low Floor Buses Due to Brake Hose Wear

    Gillig is recalling 623 Low Floor transit buses from 2013-2015 because brake hoses may rub against suspension towers, potentially causing air leaks and increased stopping distances.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2015·2015-04-14

    Beech-Nut Recalls Baby Food Jars Due to Possible Glass Contamination

    Beech-Nut Nutrition is recalling approximately 1,920 pounds of Stage 2 sweet potato and chicken baby food jars due to possible glass contamination.

    Product
    Beech-Nut Nutrition Corporation — Beech-Nut Nutrition Recalls Baby Food Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·15109·2015-04-14

    San Pedro Manufacturing Recalls Renovated Mattresses and Foundations

    San Pedro Manufacturing is recalling about 4,800 renovated mattresses and foundations because they fail to meet federal fire safety standards.

    Product
    Mattresses and Mattresses with Foundations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·060-2015·2015-04-13

    Leader Slaughterhouse Recalls Veal Carcasses Produced Without Full Federal Inspection

    Leader Slaughterhouse, LLC is recalling approximately 1,800 pounds of veal carcasses produced without the full benefit of federal inspection. The product was distributed to customers in Pennsylvania and New York.

    Product
    Leader Slaughterhouse, LLC — Leader Slaughterhouse, LLC Recalls Veal Carcasses Produced Without Full Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V215000·2015-04-13

    Crossroads Recalls 2016 Recreational Trailers Due to Wheel Stud Defect

    Crossroads is recalling 2016 recreational trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.

    Product
    CROSSROADS — CROSSROADS ELEVATION, HAMPTON, REZERVE, SUNSET TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V214000·2015-04-10

    Land Rover Recalls 2015 LR4 Models Due to ABS Software Error

    Land Rover is recalling 2015 LR4 vehicles because an ABS software error may disable stability and traction control systems, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER LR4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V211000·2015-04-10

    Spartan Recalls 2015 K3 Chassis Due to Tag Axle Suspension Defect

    Spartan Motors is recalling 66 model year 2015 K3 chassis because tag axle suspension hangers may move, causing the axle to shift off center and increasing crash risk.

    Product
    SPARTAN — SPARTAN K3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1869-2015·2015-04-08

    Horizon Cheddar Sandwich Crackers Recalled for Undeclared Peanuts

    WhiteWave Foods is recalling Horizon Cheddar Sandwich Crackers because they may contain undeclared peanuts due to a packaging error.

    Product
    Organic Horizon Sandwich Crackers Cheddar, 7.5 oz packages, 12 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1791-2015·2015-04-08

    HT Traders Blue Cheese Jalapeno Seasoning Blend Recalled for Undeclared Peanut

    Brinkhoff & Monoson Inc is recalling HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend because it may contain undeclared peanut allergens.

    Product
    HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend packaged in a 6 oz clear square glass bottle with a black metal cap and a label weight of 3.7 oz (104.9 g), Proudly Distributed by Harris Teeter, LLC., Matthews, NC;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0428-2015·2015-04-08

    Baxter Recalls Clinimix E Due to Sterility Assurance Concerns

    Baxter Healthcare is recalling 7,444 containers of Clinimix E 5/20 due to a lack of assurance of sterility and increased leak complaints.

    Product
    CLINIMIX E — CLINIMIX E (LEUCINE, PHENYLALANINE, LYSINE, METHIONINE, ISOLEUCINE, VALINE, HISTIDINE, THREONINE, TRYPTOPHAN, ALANINE, GLYCINE, ARGININE, PROLINE, SERINE, TYROSINE, DIBASIC POTASSIUM PHOSPHATE, MAGNESIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide