The Recall Desk

State

Nebraska product recalls

73,741 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.

Which agencies issued them

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40701–40725 of 78321

  • ModerateFDA (Drugs)·D-0852-2018·2018-06-20

    RIJ Recalls Gericare Diocto Liquid Due to Microbial Count Deviation

    RIJ Pharmaceutical LLC is recalling Gericare Diocto Liquid because a water sample showed an out-of-specification total aerobic microbial count.

    Product
    Gericare Diocto Liquid (Docusate Sodium 50mg), 50 mg/5 mL, packaged in 16 FL OZ (473 mL) bottles, Dist by: Gericare Pharmaceuticals Corp. 1650 63rd Street, Brooklyn, NY 11204, NDC 57896-403-16, UPC 357896-403164,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0846-2018·2018-06-20

    RIJ Pharmaceutical Recalls Gericare Acetaminophen Due to Microbial Count

    RIJ Pharmaceutical LLC is recalling Gericare Liquid Pain Relief Acetaminophen due to out-of-specification microbial counts in a water sample.

    Product
    Gericare Liquid Pain Relief Acetaminophen Cherry Flavor 160mg/5mL, packaged in 16 FL OZ (473 mL), Dist. By Gericare Pharmaceuticals 1650 63rd Street Brooklyn, NY 11204, NDC 5789618016, UPC 357896180164
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0848-2018·2018-06-20

    GeriCare Senna Syrup Recalled for Microbial Contamination

    RIJ Pharmaceutical LLC is recalling GeriCare Senna Syrup due to out-of-specification microbial counts in a water sample.

    Product
    GeriCare Senna Syrup (Sennosides 8.8 mg), 8 fl oz (237 mL) bottles, Dist, by Gericare Pharmaceuticals 1650 63rd Street Brooklyn, NY 11204, NDC 57696-452-08, UPC 357896452087
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2142-2018·2018-06-20

    Philips IntelliVue MX40 Patient Monitor Recalled for Missing Warning Statements

    Philips is recalling 7,178 IntelliVue MX40 Patient Monitors because five warning statements are missing from the instructions for use.

    Product
    IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865351
    Category
    Medical Device
    Distribution
    53 states
  • ModerateFDA (Drugs)·D-0850-2018·2018-06-20

    Geritrex Senna Syrup Recalled for Microbial Contamination

    RIJ Pharmaceutical LLC is recalling Geritrex Senna Syrup due to out-of-specification microbial counts in a water sample.

    Product
    Geritrex Senna Syrup (sennosides 8.8mg), packaged in 8 FL OZ. (236 mL) bottle, Distributed by Geritrex, LLC 144 Kingsbridge Rd East Mt Vernon, NY 10550, 1-800-736-3437, NDC 54162-007-08, UPC 354162007088
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0867-2018·2018-06-20

    MBi Homeopathic Teething Drops Recalled for Lack of Manufacturing Controls

    MBi Nutraceuticals is voluntarily recalling homeopathic teething drops and other products due to a lack of adequate controls during manufacturing.

    Product
    Teething Drops, Homeopathic Drops for Temporary Relief of Pain Caused by Teething, 1 Fl Ounce glass amber bottle with glass dropper, MBi Nutraceuticals, Lindon, UT 84042. Bar Code: 3 58301 04011 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0873-2018·2018-06-20

    MBi Nutraceuticals Recalls Homeopathic Teething and Nausea Drops

    MBi Nutraceuticals is voluntarily recalling several homeopathic products, including teething and nausea drops, due to a lack of adequate manufacturing controls.

    Product
    Silver-Zinc Throat Spray, HOMEOPATHIC IMMUNE DEFENSE, 50PPM, 4oz/50 ppm/ 120ml,amber PET bottle with white sprayer. MBi Nutraceuticals Lindon, Utah 84042 USA. Bar Code: 3 58301 18118 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0872-2018·2018-06-20

    MBi Recalls Homeopathic Products Due to Manufacturing Control Deficiencies

    MBi Distributing Inc. is voluntarily recalling several homeopathic products, including Argentum Elixir, due to a lack of adequate manufacturing controls.

    Product
    Argentum Elixir Colloidal Silver, 50 PPM Homeopathic Infection Fighter, 8 fl oz. amber PET bottle with white sprayer. MBi nutraceuticals Lindon UT, 84042. Bar COde: 3 58301 18114 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E042000·2018-06-19

    Bosch High Pressure Fuel Pump Recall for Fire Risk

    Bosch is recalling high pressure fuel pump assemblies for Ford and GM vehicles because welds may fracture, causing a fuel leak that could lead to a fire.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V413000·2018-06-19

    Forest River Recalls 2019 Prime Time Trailers Due to Stove Flame Hazard

    Forest River is recalling 2019 Prime Time recreational trailers because the stove is not isolated from the furnace return air, which can cause an inverted flame and increase the risk of injury.

    Product
    FOREST RIVER — FOREST RIVER PRIME TIME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V414000·2018-06-19

    Forest River Prime Time Recalled for Incorrect Tire Pressure Label

    Forest River is recalling 2016-2018 Prime Time recreational trailers because the Federal Placard incorrectly states tire pressure as 65 PSI instead of 80 PSI.

    Product
    FOREST RIVER — FOREST RIVER PRIME TIME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V402000·2018-06-15

    Mazda Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Mazda is recalling specific 2003-2011 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA MAZDA6, MPV, RX-8, MAZDASPEED6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V404000·2018-06-15

    Mazda Recalls MPV and RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2005-2006 MPV and 2005-2009 RX-8 vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA MPV, RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V403000·2018-06-15

    Mazda Recalls 2009-2010 RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2009-2010 RX-8 vehicles because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V410000·2018-06-15

    2017-2018 Thomas Built Buses Saf-T-Liner EFX Air Brake Recall

    Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner EFX transit buses due to a check valve defect that may cause sudden parking brake activation and increase crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E041000·2018-06-15

    Simard Suspensions Recalls Front Axles Due to Wheel Detachment Risk

    Simard Suspensions is recalling certain front suspensions because heat from brakes may melt plastic insulators, causing wheels to detach and increasing crash risk.

    Product
    SUSPENSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V407000·2018-06-15

    Mercedes-Benz Recalls 2018 S-Class Vehicles for Electrical Fire Risk

    Mercedes-Benz is recalling 2018 S-Class and Maybach vehicles because improperly secured electrical power bars in the trunk may increase the risk of a fire or loss of vehicle functions.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH, MERCEDES-BENZ S 560 4MATIC, S 650, S 450, S560
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V411000·2018-06-15

    Freightliner Recalls 2018-2019 Cascadia Trucks Due to Brake Caliper Bolt Issue

    Daimler Trucks North America is recalling 2018-2019 Freightliner Cascadia vehicles because brake caliper mounting bolts may not be properly tightened, potentially leading to reduced braking performance.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V409000·2018-06-15

    Thomas Built Buses Recalls Saf-T-Liner EFX School Buses for Brake Defect

    Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner EFX school buses because an incorrectly plumbed check valve may cause sudden parking brake activation and increase crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V405000·2018-06-15

    Mercedes-Benz Recalls 2018 GLA 250 for Missing Child Seat Anchor

    Mercedes-Benz is recalling 2018 GLA 250 vehicles because the center rear child seat tether anchor may be missing, preventing proper installation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide