The Recall Desk

State

Nebraska product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34651–34675 of 78317

  • ModerateFDA (Drugs)·D-1826-2019·2019-08-28

    Medtech Recalls Clear Eyes Assorted Displays Due to Quality Control Concerns

    Medtech Products is recalling Clear Eyes Assorted IRC Displays due to concerns about quality assurance controls in the manufacturing facility.

    Product
    Clear Eyes Assorted IRC Display; each display contains 6 each of a) Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.12%) eye drops, 0.5 FL OZ (15 mL) bottle (UPC 6 78112 25415 6); b) Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5%, Naphazoline…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2354-2019·2019-08-28

    Molded Products Recalls Mislabelled Luer Lock Sets for IV Administration

    Molded Products Inc is recalling 130,000 Luer Lock Sets (Catalog # MPC-125) because some packages were incorrectly labeled as a different product.

    Product
    Luer Lock Set - Catalog # MPC-125, for IV administration sets.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2351-2019·2019-08-28

    Siemens ACUSON NX2 Ultrasound Systems Recalled for Acoustic Output Defect

    Siemens is recalling 70 ACUSON NX2 ultrasound systems because internal testing found transducers may exceed defined acoustic output power values.

    Product
    ACUSON NX2 Elite Diagnostic Ultrasound System, Model # 11284500, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A, VA11B; UDI # 04056869050775 The ACUSON NX2 diagnostic ultrasound imaging systems are intended for the following applications…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2291-2019·2019-08-28

    FDA Recalls MICRO-TEMP LT Heat Therapy Systems Due to Tissue Damage Risk

    Cincinnati Sub-Zero is recalling 2,079 MICRO-TEMP LT heat therapy systems because updated warnings indicate that exceeding 40°C for extended periods may cause tissue damage.

    Product
    MICRO-TEMP LT System, Model 749- Localized Heat Therapy System is intended to warm a patient's body part through conductive heat transfer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E059000·2019-08-27

    Chrysler Recalls Mopar Rear Step Kits for 2019 Ram 1500 Trucks

    Chrysler is recalling Mopar Rear Step Kits for 2019 Ram 1500 trucks because they may contact the fuel tank in a rear crash, causing a leak and fire risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19188·2019-08-27

    Happy Plugs Recalls Wireless Headphones Due to Burn Hazard

    Happy Plugs is recalling Bluetooth Wireless II headphones because the included micro-USB charging cable can cause overheating and burns. No injuries have been reported.

    Product
    Happy Plugs Bluetooth Wireless II Headphones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·19773·2019-08-26

    BRP Recalls 2019 Ski-Doo Snowmobiles Due to Fuel Leak Fire Hazard

    BRP is recalling about 2,900 2019 Ski-Doo snowmobiles with 850 E-TEC engines because a fuel leak at the injector poses a fire hazard. Consumers should stop using the vehicles and contact a dealer for a free repair.

    Product
    2019 Ski-Doo snowmobiles equipped with an 850 E-TEC engine
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E057000·2019-08-26

    MAC Tools tire pressure gauges recalled due to inaccurate pressure readings

    Stanley Assembly Technologies is recalling certain MAC Tools tire pressure gauges because they may display lower than actual pressure when battery voltage is low, potentially causing tires to burst.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V623000·2019-08-26

    Lance Camper Recalls 2018-2019 855S Trailers Due to Fire Risk

    Lance Camper is recalling 2018-2019 855S trailers because a wire may contact the refrigerator burner box, increasing fire risk.

    Product
    LANCE CAMPER — LANCE CAMPER LANCE CAMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V615000·2019-08-22

    Volkswagen Recalls Vehicles Due to Ignition Key Removal Risk

    Volkswagen is recalling 679,027 vehicles because silicate buildup may allow the key to be removed when the transmission is not in Park, increasing the risk of a rollaway.

    Product
    VOLKSWAGEN — VOLKSWAGEN BEETLE, GOLF SPORTWAGEN, JETTA, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E056000·2019-08-22

    ZF Brake Calipers Recalled for Incorrect Assembly Fluid and Drag Risk

    ZF North America is recalling brake calipers that may contain incorrect assembly fluid, causing seals to swell and brakes to drag.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:CALIPER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V618000·2019-08-22

    Peterbilt 337 and 348 Trucks Recalled for Steering Column Defect

    PACCAR is recalling 2019-2020 Peterbilt 337 and 348 trucks because a steering shaft weld may crack, causing loss of steering control.

    Product
    PETERBILT — PETERBILT 348, 337
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V620000·2019-08-22

    Thomas Built Minotour School Buses Recalled for Missing Backup Cameras

    Daimler Trucks North America is recalling 2019-2020 Thomas Built Minotour school buses because they may be missing backup cameras, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2064-2019·2019-08-21

    Fenwal Volumat MC Agilia Infusion Pump Software Recall

    Fenwal Inc is recalling Volumat MC Agilia infusion pumps to correct four software anomalies and an alarm priority issue in specific software versions.

    Product
    VOLUMAT MC AGILIA US, Infusion Pump, REF Z021135, software versions 1.7 and 1.9a Product Usage: The Volumat MC Agilia is a piece of transportable medical equipment intended to be used in healthcare facilities environment by healthcare trained professionals according to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2264-2019·2019-08-21

    Degania Silicone Recalls Jackson-Pratt Channel Drains Due to Breakage Risk

    Degania Silicone is recalling Cardinal Health Jackson-Pratt Channel Drains because they may break during use, requiring additional surgery to remove the broken end.

    Product
    Cardinal Health Jackson-Pratt Channel Drain 19FR, Full flutes, with trocar Cardinal Health: PN: JP-2191 An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1820-2019·2019-08-21

    American Health Packaging Recalls Aspirin and Dipyridamole Capsules

    American Health Packaging is recalling specific lots of Aspirin and Extended-release Dipyridamole Capsules due to an unknown impurity found in stability samples.

    Product
    Aspirin and Extended-release Dipyridamole Capsules, 25 mg/200 mg, 20 capsules per carton (5 blister cards x 4 unit doses), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-305-32; NDC Blister Pack: 60687-305-33
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2261-2019·2019-08-21

    Cardinal Health Jackson-Pratt Channel Drain Recall for Breakage Risk

    Degania Silicone is recalling Cardinal Health Jackson-Pratt Channel Drains because they may break during use or removal, requiring additional surgery.

    Product
    Cardinal Health Jackson-Pratt Channel Drain 15FR, Full flutes Cardinal Health PN: JP-2188 An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels…
    Category
    Medical Device
    Distribution
    Distributed nationwide