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.

45426–45450 of 78389

  • ModerateFDA (Drugs)·D-0944-2017·2017-07-12

    GSK Recalls Parodontax Toothpaste Due to Possible Metal Presence

    GSK Consumer Healthcare is recalling 15,708 tubes of Parodontax Whitening toothpaste due to the possibility of metal in the product.

    Product
    PARODONTAX — PARODONTAX (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0934-2017·2017-07-12

    PharMEDium Recalls Ropivacaine HCl Injection Due to Labeling Errors

    PharMEDium Services, LLC is recalling 21 pumps of Ropivacaine HCl 0.2% injection due to incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0935-2017·2017-07-12

    PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling two Bupivacaine HCl ON-Q pumps due to incorrect or missing lot and expiration date labeling.

    Product
    Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 270 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-044-57
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2659-2017·2017-07-12

    Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-Packaging

    Encore Medical is recalling 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.

    Product
    3DKNEE(TM) SYSTEM e+, Tibial Insert, RIGHT Sz 8 / 11mm, REF 391-11-708, QTY 01 The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0932-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors

    PharMEDium Services is recalling 147 Ropivacaine HCl IV pumps nationwide because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0930-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling 79 Ropivacaine HCl IV pumps because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-256-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0936-2017·2017-07-12

    PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling seven Bupivacaine HCl ON-Q pumps because of incorrect or missing lot and expiration dates.

    Product
    Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-023-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0931-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors

    PharMEDium Services is recalling 22 Ropivacaine HCl pumps nationwide because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0933-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Lot and Expiration Dates

    PharMEDium Services, LLC is recalling 10 Ropivacaine HCl 0.2% ON-Q pumps nationwide due to incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 750 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 600 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-279-33
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E034000·2017-07-10

    Takata Driver Frontal Air Bag Inflator Recall for Rupture Risk

    Takata is recalling specific driver-side air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V435000·2017-07-10

    Chrysler Recalls 2011-2014 Vehicles for Alternator Failure Risk

    Chrysler is recalling specific 2011-2014 Dodge, Chrysler, and Jeep vehicles because the alternator may fail, causing the vehicle to stall or catch fire.

    Product
    DODGE — DODGE, CHRYSLER, JEEP DURANGO, 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V437000·2017-07-10

    GM Recalls 40,683 Vehicles for Air Bag and Seat Belt Software Defect

    General Motors is recalling 40,683 vehicles from 2014-2017 because a software error may prevent front air bags and seat belt pretensioners from deploying in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC, BUICK CORVETTE, SILVERADO 1500, SIERRA 1500, LACROSSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V438000·2017-07-10

    BMW Recalls 2014-2017 R1200GS Motorcycles for Fork Tube Separation Risk

    BMW is recalling 2014-2017 R1200GS and R1200GS Adventure motorcycles because the fixed fork tube may separate from the seal plug, increasing crash risk.

    Product
    BMW — BMW R1200 GS ADVENTURE, R 1200 GS ADVENTURE, R1200 GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E036000·2017-07-10

    MORryde Recalls Jerry Can Holders for Detachment Risk

    MORryde is recalling Jerry Can holders that may tear apart from the spare tire mount, creating a road hazard.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V434000·2017-07-07

    Chrysler Recalls 2017 Ram 1500 Trucks for Fuel Tank Valve Defect

    Chrysler is recalling 2017 Ram 1500 trucks because a broken fuel tank control valve may leak fuel if the vehicle is inverted, increasing fire risk in a rollover crash.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V431000·2017-07-07

    2017 Dodge Challenger Recall for Transmission Park Position Defect

    Chrysler is recalling 2017 Dodge Challengers with 5.7L V8 engines and eight-speed automatic transmissions because the vehicle may not stay in Park, increasing crash risk.

    Product
    DODGE — DODGE CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V432000·2017-07-07

    Dodge Journey Recall for Frontal Air Bag Wiring Defect

    Chrysler is recalling 2011-2015 Dodge Journey vehicles because the driver's frontal air bag wiring may chafe and short circuit, causing unexpected deployment.

    Product
    DODGE — DODGE JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V433000·2017-07-07

    2017 Jeep Compass Recall for Incorrect Jump Start Instructions

    Chrysler is recalling 2017 Jeep Compass vehicles because the User's Guide contains reversed battery terminal polarity for jump starting, which may increase the risk of injury.

    Product
    JEEP — JEEP COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V430000·2017-07-06

    Forest River Recalls Transit Buses Due to Driveshaft Coupling Failure Risk

    Forest River is recalling specific 2015-2018 transit buses and work trucks because a flexible coupling may fail, potentially damaging brake and fuel lines.

    Product
    STARCRAFT — STARCRAFT, FOREST RIVER, GLAVAL PRODIGY BUS, STARLITE, CANDIDATE II, CROSSFIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V427000·2017-07-06

    Ford Recalls 2017 Edge, Fusion, and Lincoln MKZ for Torque Converter Defect

    Ford is recalling 2017 Edge, Fusion, and Lincoln MKZ vehicles with 2.0L engines and six-speed automatics because torque converter weld studs may be inadequate, risking loss of vehicle movement.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide