The Recall Desk

State

Nebraska product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36751–36775 of 78318

  • ModerateFDA (Drugs)·D-1079-2019·2019-04-10

    KRS Global Biotechnology Recalls NORepinephrine IV Bags Due to Labeling Error

    KRS Global Biotechnology is recalling 433 bags of NORepinephrine 4 mg in 5% Dextrose due to a label mix-up. The product was distributed nationwide.

    Product
    NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF), 4 mg / 250 mL, 250 mL IV bag, Rx only, KRS Global Biotechnology: 791 Park of Commerce Blvd., Boca Raton, FL 33487. NDC 3321674481
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1076-2019·2019-04-10

    Abbott ARCHITECT Creatine Kinase IVD Recalled for Stability Issues

    Abbott Laboratories is recalling 30 kits of ARCHITECT Creatine Kinase IVD due to a stability issue that may cause error codes or out-of-range quality control results.

    Product
    Abbott ARCHITECT Creatine Kinase, IVD, REF 7D6341.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1074-2019·2019-04-10

    Abbott Recalls CELL-DYN Emerald Analyzers Due to Quality Control Errors

    Abbott Laboratories is recalling 6,353 CELL-DYN Emerald analyzers worldwide because they may generate incorrect low quality control results for red blood cells and platelets.

    Product
    CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is an automated hematology analyzer intended for in-vitro diagnostic use in the clinical laboratory.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1068-2019·2019-04-10

    Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures

    Pfizer is recalling specific lots of Cleocin Phosphate injection because high out-of-specification impurity levels were detected at the 24-month time point.

    Product
    CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1088-2019·2019-04-10

    Beaver Visitec Recalls Micro Knife 5.0mm Due to Misprinted Expiration Date

    Beaver Visitec is recalling 97 boxes of Micro Knife 5.0mm 30° instruments because the expiration date was misprinted as the lot number.

    Product
    Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for ophthalmic, ENT and other forms of surgery stab incisions and other microsurgical techniques. .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1067-2019·2019-04-10

    Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures

    Pfizer is recalling specific lots of Cleocin Phosphate injection because high out-of-specification impurities were detected at the 24-month time point.

    Product
    CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V283000·2019-04-09

    Proterra Recalls 2015-2018 Catalyst Buses Due to Brake Fire Risk

    Proterra is recalling 2015-2018 Catalyst 40 buses because a clogged tow fitting cap can cause rear brakes to overheat and catch fire.

    Product
    PROTERRA — PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V282000·2019-04-09

    Peterbilt 520 Recall: Undersized Wires May Cause Engine Shutdown

    PACCAR is recalling 2017-2020 Peterbilt 520 trucks because undersized wires may overheat and melt, potentially causing an unexpected engine shutdown and increasing crash risk.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V281000·2019-04-09

    Horton Ambulances Recalled for Reversed Backup Camera Image

    Halcore Group is recalling 2016-2019 Horton ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    HORTON — HORTON TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V284000·2019-04-09

    Daimler Recalls 2019 Sprinter Vans for Headlight Sensor Calibration Issues

    Daimler Vans USA is recalling 2019 Freightliner and Mercedes-Benz Sprinter vans because the headlamp range adjustment sensor may not be calibrated, potentially affecting driver visibility.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V276000·2019-04-09

    AEV TraumaHawk Ambulances Recalled for Reversed Backup Camera Image

    Halcore Group is recalling 2016-2019 AEV TraumaHawk ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V280000·2019-04-09

    Pierce Frontline Vehicles Recalled for Brake Light Wiring Defect

    Pierce is recalling 2018-2019 Frontline C-35X, C-25, C-45X-3, and Encore Rescue vehicles because brake lights may illuminate without the pedal being pressed.

    Product
    FRONTLINE — FRONTLINE C-35X, C-25, ENCORE RESCUE, C-45X-3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19102·2019-04-09

    Marpac Recalls GO Travel Sleep Sound Machines Due to Burn Hazard

    Marpac is recalling GO travel sleep sound machines because the internal battery can leak and cause an electrical short, posing a burn hazard.

    Product
    GO travel sleep sound machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V279000·2019-04-08

    Load Trail Recalls 2018-2019 Dump Trailers Due to Bolt Failure Risk

    Load Trail is recalling 2018-2019 dump trailers because bolts on the hydraulic cylinder can break under heavy loads, causing the dump box to lower rapidly.

    Product
    LOAD TRAIL — LOAD TRAIL TANDEM AXLE DUMP, TRIPLE AXLE DUMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V278000·2019-04-08

    Ford Recalls F-Series Trucks Due to Block Heater Fire Risk

    Ford is recalling 2015-2019 F-150 and 2017-2019 Super Duty trucks because a damaged block heater cable could cause a fire.

    Product
    FORD — FORD F-250 SD, F-350 SD, F-150, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V274000·2019-04-05

    Nova Bus Recalls 2011-2019 LFS City Buses for Fire Risk

    Nova Bus is recalling 2011-2019 LFS city buses because an engine door fan electrical connector may overheat and cause a fire.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·042-2019·2019-04-05

    J&J Snack Foods Recalls Stuffed Sandwiches Due to Plastic Contamination

    J&J Snack Foods Handhelds Corp. is recalling Bremer hot stuffed sandwiches due to possible semi-transparent plastic contamination. No illnesses have been reported.

    Product
    J&J Snack Foods Handhelds Corp. — J&J Snack Foods Handhelds Corp. Recalls Stuffed Sandwich Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V275000·2019-04-05

    Kenworth T680 and T880 Recalled for Parking Brake Signal Delay

    PACCAR is recalling 2018-2020 Kenworth T680 and T880 trucks because a parking brake signal delay in cold weather may cause unexpected vehicle movement.

    Product
    KENWORTH — KENWORTH T680, T880
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V273000·2019-04-04

    BMW Recalls 2006 Models Due to PCV Valve Fire Risk

    BMW is recalling 2006 3, 5, and Z4 series vehicles because a heater in the PCV valve may short circuit, increasing the risk of a fire.

    Product
    BMW — BMW Z4, 530XI, 525I, 325XI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·041-2019·2019-04-04

    Blount Fine Foods Recalls Chicken Soup for Undeclared Milk Allergen

    Blount Fine Foods is recalling frozen chicken soup products due to misbranding and an undeclared milk allergen. No adverse reactions have been reported.

    Product
    Blount Fine Foods — Blount Fine Foods Recalls Ready-To-Eat Chicken Soup Product due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·19099·2019-04-04

    Vivitar Recalls Hot/Cold Massage Balls Due to Burn Hazard

    Vivitar is recalling hot/cold massage balls sold at Target because they can leak or rupture during microwaving, posing a burn hazard.

    Product
    Hot/cold massage balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1085-2019·2019-04-03

    Blue Fusion Capsules Recalled for Undeclared Prescription Ingredients

    Ata International Inc is recalling Blue Fusion Capsules because FDA analysis found undeclared prescription ingredients, including Sildenafil and Tadalafil.

    Product
    Blue Fusion Capsules, 1- count blister pack, Distributed by: DNS Distribution 5225 Canyon Crest Dr. Ste 71-640, Riverside, CA 92507, UPC 7 48252 66460 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0986-2019·2019-04-03

    Maquet Cardiohelp Emergency Drive Recalled for Gearwheel Assembly Defect

    Maquet Cardiovascular is recalling 10 units of the Cardiohelp Emergency Drive because the gearwheel may have been incorrectly reassembled, leading to inadequate operation.

    Product
    Cardiohelp Emergency Drive, Part No. 70104.8002 Product Usage: The Cardiohelp Emergency Drive is used in emergencies to manually drive the disposable if the Cardiohelp-i fails.
    Category
    Medical Device
    Distribution
    Distributed nationwide