The Recall Desk

State

Nebraska product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51226–51250 of 78397

  • LowFDA (Drugs)·D-1441-2016·2016-07-20

    West-Ward Recalls Oxycodone Hydrochloride Oral Solution for Impurity Failures

    West-Ward Columbus Inc. is recalling 1,182 bottles of Oxycodone Hydrochloride Oral Solution due to failed impurities and degradation specifications.

    Product
    OXYCODONE HYDROCHLORIDE — OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V543000·2016-07-19

    Blue Bird Vision Transit Buses Recalled for Propane Fuel Line Defect

    Blue Bird is recalling 2016-2017 Vision transit buses with 6.8L Ford engines and Gen 3 propane units because fuel lines may rub, causing leaks and fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V541000·2016-07-19

    Ditch Witch T14MV Trailer Recalled for Brake Wiring Defect

    Charles Machine Works is recalling 2016 Ditch Witch T14MV trailers because an incorrect wiring harness may prevent brakes from applying if the trailer separates from the tow vehicle.

    Product
    DITCH WITCH — DITCH WITCH T14MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V540000·2016-07-19

    BMW Recalls 2015 M5 and M6 Models for Driveshaft Weld Defect

    BMW is recalling 956 model year 2015 M5 and M6 vehicles because a defective driveshaft weld may cause loss of propulsion or vehicle rolling, increasing crash risk.

    Product
    BMW — BMW M6, M5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V537000·2016-07-19

    Spartan Motors Recalls Transit Bus Chassis Cabs Due to Frame Cracks

    Spartan Motors is recalling 2011-2015 Transit Bus Chassis Cabs because frames may crack, potentially reducing driver control and increasing crash risk.

    Product
    SPARTAN MOTORS — SPARTAN MOTORS TRANSIT BUS CHASSIS CAB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2016·2016-07-19

    Bar-S Foods Recalls Chicken and Pork Hot Dogs Due to Listeria Risk

    Bar-S Foods is recalling approximately 372,684 pounds of chicken and pork hot dog and corn dog products due to possible Listeria monocytogenes contamination.

    Product
    Bar-S Foods Company — Bar-S Foods Company Recalls Chicken and Pork Hot Dog and Corn Dog Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·16227·2016-07-19

    GSI Outdoors Recalls Children's Water Bottles for Lead Violation

    GSI Outdoors is recalling about 6,700 children's insulated water bottles sold at L.L.Bean because lead solder at the base violates safety standards.

    Product
    Kids' insulated water bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V538000·2016-07-19

    Starcraft RV Recalls AR-ONE Maxx Trailers for Incorrect Tire Labeling

    Starcraft RV is recalling 2016-2017 AR-ONE Maxx travel trailers and fifth wheels because incorrect tire labels may lead to improper tire replacement.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE MAXX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16228·2016-07-19

    Things Remembered Recalls Children's Jewelry Due to Lead Violation

    Things Remembered is recalling silver bracelets and charm necklaces for children because the clear surface coating contains lead in excess of allowable limits.

    Product
    Silver bracelets and charm necklaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·056-2016 EXP·2016-07-15

    ConAgra Recalls Frozen Chicken and Beef Entrées Due to Metal Contamination

    ConAgra Foods is recalling approximately 195,597 pounds of frozen P.F. Chang's Home Menu chicken and beef products due to potential metal contamination. No injuries have been reported.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — ConAgra Foods Recalls Frozen Chicken and Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·16757·2016-07-15

    Nestlé AccuPure Water Dispensers Recalled for Fire and Burn Hazards

    Nestlé Waters North America is recalling AccuPure countertop water dispensers because they can overheat, melt, and smoke, posing fire and burn risks.

    Product
    AccuPure countertop filtered water dispensers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16223·2016-07-14

    Flushmate III Pressure-Assist Flushing Systems Recalled for Bursting Hazard

    Flushmate is recalling about 453,000 Flushmate III Pressure-Assist Flushing Systems in the U.S. because the units can burst, posing impact and laceration hazards.

    Product
    Flushmate® III Pressure-Assist Flushing Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16224·2016-07-14

    Home Source Recalls Floor Lamps Due to Fire and Shock Hazards

    Home Source is recalling about 2,700 floor lamps sold in the New York area and online because defective sockets can cause fires and electric shocks.

    Product
    Floor lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V536000·2016-07-14

    Altec Recalls 2015-2016 Aerial Devices and Digger Derricks for Winch Defect

    Altec is recalling 252 model year 2015-2016 Aerial Devices and Digger Derricks because a hydraulic motor shaft may fail, causing unexpected winch movement and increasing injury risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16226·2016-07-14

    IKEA Recalls Safety Gates and Extensions Due to Fall Hazard

    IKEA is recalling PATRULL safety gates and extensions because the locking mechanism can open unexpectedly, posing a fall hazard to children.

    Product
    Safety gates and safety gate extensions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16225·2016-07-14

    Liquid Plumr Clog Removers Recalled for Non-Child-Resistant Caps

    The Clorox Company is recalling three Liquid Plumr clog remover products because the bottles lack required child-resistant closures, posing a risk of chemical burns.

    Product
    Liquid Plumr® Pro-Strength Foaming Clog Fighter®, Liquid Plumr® Industrial Strength Urgent Clear® and Liquid Plumr® Pro-Strength Urgent Clear® clog removers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1149-2016·2016-07-13

    XCEL Capsules Recalled for Undeclared Fluoxetine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling XCEL Capsules marketed as a dietary supplement because they contain undeclared fluoxetine and phenolphthalein.

    Product
    XCEL Capsules, 300 mg, 60-count bottles, Manufactured for JNS Health
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1145-2016·2016-07-13

    Prime Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling Prime Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.

    Product
    Prime Capsules, 500mg, 60-count bottles, Distributed By Zagonfly 3129 25th St. #392 Columbus, IN 47203
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1144-2016·2016-07-13

    Oasis Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling Oasis Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.

    Product
    Oasis Capsules, 500mg, 45-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando FL 32801 (407)930-4043
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1151-2016·2016-07-13

    ZI XIU TANG Beauty Capsules Recalled for Undeclared Sibutramine

    Bee Extremely Amazed LLC is recalling ZI XIU TANG Beauty Face & Figure Capsules because they contain undeclared sibutramine, a withdrawn drug.

    Product
    ZI XIU TANG BEAUTY FACE & FIGURE Capsules, 250 mg, 60-count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1143-2016·2016-07-13

    La' Trim Plus Capsules Recalled for Undeclared Withdrawn Ingredients

    Bee Extremely Amazed LLC is recalling La' Trim Plus Capsules because the product contains undeclared sibutramine and phenolphthalein, both withdrawn from the US market for safety reasons.

    Product
    La' Trim Plus Capsules, 350 mg, 60-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando, FL 32801 (407) 930-4043
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1654-2016·2016-07-13

    Harris Teeter Soup Mix Recalled for Listeria Risk

    The Pictsweet Company is recalling Harris Teeter brand Soup Mix Veggies due to the possibility of Listeria monocytogenes contamination in the onions.

    Product
    Harris Teeter(TM) brand SOUP MIX VEGGIES, carrots, potatoes, corn, green beans, lima beans, okra, green peas, celery, onions, NET WT 12 OZ (340g), UPC 72036 71683, PROUDLY DISTRIBUTED BY HARRIS TEETER, LLC, MATTHEWS, NC 28105
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1137-2016·2016-07-13

    Hospira Recalls Magnesium Sulfate Injection Due to Particulate Matter

    Hospira Inc. is recalling specific lots of Magnesium Sulfate Injection due to confirmed particulate matter. The recall covers 88,500 vials distributed in the US and several Middle Eastern countries.

    Product
    Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.
    Category
    Drug
    Distribution
    Distributed nationwide