The Recall Desk

State

Nebraska product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32676–32700 of 78314

  • HighFDA (Devices)·Z-0681-2020·2020-01-08

    DeWALT and Stanley Laser Distance Measurers Recalled for Excessive Radiation

    Stanley Black & Decker is recalling specific DeWALT and Stanley laser distance measurers because they may emit laser radiation exceeding Class II safety limits.

    Product
    The products involved are DeWALT laser distance measurers, model numbers DW0165, DW0165S, DW0330S and Stanley Fatmax FMHT77506. These products were produced for DeWALT and Stanley by a contract manufacturer.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0749-2020·2020-01-08

    Roche Recalls Accu-Chek Guide Blood Glucose Meters Due to Power Issues

    Roche Diabetes Care is recalling 21,094 Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues. The recall covers units distributed in the US and 34 other countries.

    Product
    Blood Glucose Monitoring System, Model Number 07400942001 ACCU-CHEK GUIDE METER ONLY MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2020·2020-01-08

    Roche Recalls Accu-Chek Guide Blood Glucose Monitoring Systems

    Roche Diabetes Care is recalling specific Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues.

    Product
    Blood Glucose Monitoring System, Model Number 08453071001 ACCU-CHEK GUIDE RETAIL KIT FCN MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0751-2020·2020-01-08

    Roche Recalls Accu-Chek Guide Blood Glucose Monitoring Systems Due to Power Issues

    Roche Diabetes Care is recalling 355,400 Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues. The recall covers units distributed in the US and 33 other countries.

    Product
    Blood Glucose Monitoring System, Model Number 08453063001 ACCU-CHEK GUIDE SAMPLE KIT FCN MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0448-2020·2020-01-08

    Sara Lee Frozen Pumpkin Spice Latte Pie Recalled for Undeclared Red Dye

    Sara Lee Frozen Foods is recalling Chef Pierre Pumpkin Spice Latte Pies because they contain undeclared FD & C Red 40 dye.

    Product
    Chef Pierre 37 Ounce Pumpkin Spice Latte Pie, in foil pie pan with dome lid, frozen, 4 pies per wholesale case, with SKU number 09368 and UPC number 032100093682
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Drugs)·D-0647-2020·2020-01-08

    Akorn Recalls Myorisan 20mg Capsules Due to Mispackaging Error

    Akorn, Inc. is recalling Myorisan (isotretinoin) 20mg capsules because some cartons contained 40mg blister cards. The error was found in a customer complaint.

    Product
    MYORISAN (isotretinoin capsules, USP), 20mg, packaged in 30-count Capsules (3 x 10 Prescription Packs) per box, Rx only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forset, IL 60045; NDC 61748-302-13.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0771-2020·2020-01-08

    Nidek Specular Microscope Recalled for Electromagnetic Noise Exceeding Standards

    Nidek, Inc. is recalling 13 Specular Microscopes, Model CEM-530, because their electromagnetic noise exceeded the upper limit of the Electromagnetic Compatibility Standard.

    Product
    NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image capture of endothelium enabling observation of the size and shape of cells. Information such as the number of endothelial cells, cell density, and cell area is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0635-2020·2020-01-08

    Lupin Recalls Bimatoprost Ophthalmic Solution Due to Impurity Specifications

    Lupin Pharmaceuticals is recalling 2,130 bottles of Bimatoprost Ophthalmic Solution because an out-of-specification impurity was detected.

    Product
    Bimatoprost Ophthalmic Solution, 0.03%, For Use in the Eyes Only, Sterile, Rx Only, 7.5 mL bottle, Manufactured by: Lupin Limited, Pithampur (M.P.), INDIA, NDC: 68180-429-03.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·20V005000·2020-01-06

    Micro Bird Recalls 2015-2019 T-Series Buses for Fire Risk

    Micro Bird is recalling 2015-2019 T-Series school buses because an oversized circuit breaker may cause wire overheating and fire.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V004000·2020-01-06

    Micro Bird Recalls CT-Series Shuttle Buses Due to Fire Risk

    Micro Bird is recalling 2015-2019 CT-Series shuttle buses because an oversized breaker may cause wire overheating and fire. Owners should contact the manufacturer for a free replacement.

    Product
    MICRO BIRD — MICRO BIRD CT-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V001000·2020-01-02

    Subaru and Saab Vehicles Recalled for Air Bag Inflator Defect

    Subaru is recalling specific 2003-2014 models and Saab 9-2X vehicles because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E001000·2020-01-02

    Takata Frontal Air Bag Inflators Recalled for Explosion Risk

    Takata is recalling specific non-desiccated frontal air bag inflators used as interim remedies. These inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V003000·2020-01-02

    Subaru and Saab Recall Vehicles Due to Air Bag Inflator Defect

    Subaru is recalling specific 2003-2014 models and Saab 9-2X vehicles because passenger air bag inflators may explode, posing a risk of serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V002000·2020-01-02

    Subaru and Saab Recall Vehicles Due to Air Bag Inflator Defect

    Subaru and Saab are recalling specific model years because passenger air bag inflators may explode due to humidity, posing a risk of serious injury.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-01022020·2020-01-02

    USDA Alerts on Sun Foods Egg Products Linked to Listeria Outbreak

    USDA issued a public health alert for Sun Foods egg products containing ingredients from an FDA recall due to possible Listeria monocytogenes contamination.

    Product
    Sun Foods — FSIS Issues Public Health Alert for Products Associated with the FDA Almark Foods Recall Due to Possible Listeria Monocytogenes Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0417-2020·2020-01-01

    FDA Recalls Okami California Rolls for Listeria Contamination Risk

    Fuji Food Products is recalling Okami brand 8pc California Rolls due to potential Listeria monocytogenes contamination. Consumers should not eat the product.

    Product
    Okami brand 8pc California Roll, SKU 28101
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0422-2020·2020-01-01

    FDA Recalls Okami Spicy Supreme California Rolls for Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Spicy Supreme California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Okami brand 8pc Spicy Supreme California Roll, SKU 28104
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0414-2020·2020-01-01

    Trader Joe's Tempura Shrimp Crunch Roll Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's 8pc Tempura Shrimp Crunch Roll due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8pc Tempura Shrimp Crunch Roll, 8.5oz, SKU 513289
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0413-2020·2020-01-01

    Trader Joe's California Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's 8pcs Regular California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8pcs Regular California Roll, 8oz, SKU 00348997T
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0416-2020·2020-01-01

    Trader Joe's Brown Rice California Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's Brown Rice California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8pcs Brown Rice California Roll, 8oz, SKU 909822
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0430-2020·2020-01-01

    Trader Joe's Smoked Salmon Poke Bowl Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's 8.4oz Smoked Salmon Poke Bowls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8.4oz Smoked Salmon Poke Bowl, SKU 603751
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0418-2020·2020-01-01

    Fuji Food Products Recalls Okami Supreme California Rolls for Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Supreme California Rolls due to potential Listeria monocytogenes contamination. Consumers should not eat the product.

    Product
    Okami brand 8pc Supreme California Roll, SKU 28103
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0420-2020·2020-01-01

    Fuji Food Products Recalls Okami Spicy California Rolls for Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Spicy California Rolls due to potential Listeria monocytogenes contamination. Consumers should discard or return the product.

    Product
    Okami brand 8pc Spicy California Roll, SKU 28102
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0424-2020·2020-01-01

    Okami Brown Rice California Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Brown Rice Classic California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Okami brand 8pc Brown Rice Classic California Roll, SKU 28122
    Category
    Food
    Distribution
    31 states