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.

Which agencies issued them

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.

34676–34700 of 78317

SevereFDA (Food)·F-1994-2019·2019-08-21
Mountain Rose Herbs Recalls Fennel Seed for Salmonella Risk
Mountain Rose Herbs is recalling Fennel Whole Seed due to potential Salmonella contamination. The product was sold in the US and Canada.
Product
Fennel Whole Seed was packaged in a clear plastic bag or poly-woven bags sold in bulk form, net weight ranges from 4 ounces to 50 pounds, sold under Mountain Rose Herbs brand. The label is read in parts: "***Fennel Seed Whole ***NET WT *** Origin: Egypt *** MOUNTAIN ROSE…
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·19V616000·2019-08-21
Mack Recalls 2015 Pinnacle Trucks Due to Front Axle Fracture Risk
Mack Trucks is recalling 2015 Pinnacle (CXU) vehicles because front steer axles may have missed a heat-treating step, potentially causing them to fracture and leading to a loss of vehicle control.
Product
MACK — MACK PINNACLE (CXU)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V614000·2019-08-21
Volkswagen Recalls 2019 Atlas Vehicles Due to Fuel Tank Weld Defect
Volkswagen is recalling 2019 Atlas vehicles because a fuel tank weld defect may cause fuel leaks or engine stalling, increasing fire and crash risks.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2260-2019·2019-08-21
Degania Silicone Jackson-Pratt Channel Drain Recall for Breakage Risk
Degania Silicone is recalling 640 units of Jackson-Pratt Channel Drains because they may break during use or removal, requiring additional surgery.
Product
Cardinal Health Jackson-Pratt Channel Drain 15FR Cardinal PN:JP-2223 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, drain fluids from…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2263-2019·2019-08-21
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, requiring additional surgery.
Product
Cardinal Health Jackson-Pratt Channel Drain 19FR, Full flutes Cardinal Health: PN JP-2190 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
SevereFDA (Devices)·Z-2065-2019·2019-08-21
Fenwal Recalls Vigilant Agilia and Volumat MC Agilia Infusion Pump Software
Fenwal Inc is recalling 83 units of Vigilant Agilia and Volumat MC Agilia software to correct four anomalies and an alarm priority issue.
Product
Vigilant Agilia, Vigilant Drug'Lib, REF Z073476, versions 1.0 and 1.1 Product Usage: Vigilant Drug Lib is Dose Error Reduction Software that, when used in combination with Volumat MC Agilia infusion pumps, is intended to reduce drug administration errors at the bedside.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2262-2019·2019-08-21
Degania Silicone Jackson-Pratt Channel Drain Recall for Breakage Risk
Degania Silicone is recalling 6,080 units of Cardinal Health Jackson-Pratt Channel Drains because they may break during use, requiring additional surgery.
Product
Cardinal Health Jackson-Pratt Channel Drain 15FR, Full flutes, with trocar Product Number: JP-2189 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 (Devices)·Z-2265-2019·2019-08-21
Degania Silicone Recalls Jackson-Pratt Channel Drains Due to Breakage Risk
Degania Silicone is recalling 2,160 units of Cardinal Health Jackson-Pratt Channel Drains because they may break during use, potentially requiring additional surgery.
Product
Cardinal Health Jackson-Pratt Channel Drain 19FR, 3/4 flutes, with trocar Cardinal Health: PN JP-2225 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 (Devices)·Z-2266-2019·2019-08-21
Medline Silicone Drain Recalled for Risk of Breaking During Use
Degania Silicone is recalling 200 units of Medline Silicone Drains because they may break during use, requiring additional surgery to remove the broken end.
Product
Medline Silicone Drain 15Fr 3/16" Full Fluted PN: DYNJWE2188HB 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, drain fluids from body…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2267-2019·2019-08-21
Smith & Nephew Wound Drain Recall Due to Breakage Risk
Smith & Nephew is recalling 15FR and 19FR channel wound drains because they may break during use or removal, requiring additional surgery.
Product
Smith & Nephew Negative Pressure Wound Therapy 15FR Channel Wound Drain PN: 02872 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, drain…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V617000·2019-08-21
Volvo Recalls 2015 VNL Trucks for Front Axle Fracture Risk
Volvo Trucks North America is recalling 2015 VNL trucks because front axles may fracture due to missed heat treating, increasing crash risk.
Product
VOLVO — VOLVO VNL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2245-2019·2019-08-21
BioPro K-Wire Single Trocar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 240 units of K-Wire Single Trocar 2.5x150mm due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Single Trocar 2.5x150mm, Item Number OL15025S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2254-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x32 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x32, Item Number 19652 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2285-2019·2019-08-21
Luminex ARIES GBS Assay Recalled for Partially Sealed Side Cassettes
Luminex Corporation is recalling ARIES GBS Assay kits because partially sealed side cassettes may cause decreased assay sensitivity or stability.
Product
ARIES GBS Assay , REF 50-10021, UDI # 00840487100165
Category
Medical Device
Distribution
34 states
HighNHTSA·19V611000·2019-08-21
Keystone Recalls 2019-2020 Hideout 25TH Toy Haulers for Missing Warning Label
Keystone RV Company is recalling 2019-2020 Hideout 25TH toy haulers because they may be missing a required warning label in the garage area.
Product
KEYSTONE — KEYSTONE HIDEOUT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2240-2019·2019-08-21
BioPro K-Wire Sterile Single Trochar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling K-Wire Sterile Single Trochar units due to a manufacturing flaw in the sterile barrier system that may compromise sterility.
Product
K-Wire Sterile Single Trochar, Item Number 19106 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2230-2019·2019-08-21
Elekta iGUIDE System Recalled for Potential Position Monitoring Error
Elekta is recalling 374 iGUIDE Systems because they may incorrectly monitor 3D position. The recall covers devices distributed nationwide and worldwide.
Product
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2253-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x115 due to a manufacturing flaw in the sterile barrier system. The devices are intended for orthopedic surgical procedures.
Product
Go-EZ Screw 6.5x115, Item Number 19671 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2242-2019·2019-08-21
BioPro K-Wire Single Trocar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 350 units of K-Wire Single Trocar 2.5x170mm due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Single Trocar 2.5x170mm, Item Number OL17025S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2259-2019·2019-08-21
BioPro K-Wire HBS Sterile Lots Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 17 units of K-Wire HBS Sterile Lots due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire HBS Sterile Lot, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2246-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Flaw
BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x30 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x30, Item Number 19651 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2271-2019·2019-08-21
Siemens SOMATOM Drive CT Systems Recalled for Software Safety Issues
Siemens Medical Solutions is recalling SOMATOM Drive CT systems due to four software issues that may cause scan aborts.
Product
SOMATOM Drive, Model Number 10431700 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2055-2019·2019-08-21
Amy's Kitchen Recalls Broccoli and Cheddar Bake Due to Foreign Material
Amy's Kitchen Inc. is recalling 5,207 cases of Broccoli & Cheddar Bake due to consumer complaints of black plastic found in the product.
Product
Amy's Bowls - Broccoli & Cheddar Bake; Net Wt. 9.5 oz. (269g) Perishable - Keep Frozen. Microwave or regular oven. UPC: 0 42272 00811 7 Amy's kitchen Inc., P.O. Box 7129, Petaluma, CA 94955 INGREDIENTS: RICE PASTA (ORGANIC RICE FLOUR, FILTERED WATER, ORGANIC POTATO…
Category
Food
Distribution
27 states
HighNHTSA·19V612000·2019-08-21
Rolls-Royce Cullinan Recall for Dim Brake Lights
BMW is recalling 2019 Rolls-Royce Cullinan vehicles because brake lights may not be bright enough, increasing crash risk.
Product
ROLLS-ROYCE — ROLLS-ROYCE CULLINAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2270-2019·2019-08-21
Siemens SOMATOM CT Systems Recalled for Software Scan Abort Risk
Siemens is recalling SOMATOM Definition Flash CT systems due to four software issues that may cause scans to abort.
Product
SOMATOM Definition Flash, Model Number 10430603 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained…
Category
Medical Device
Distribution
Distributed nationwide