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.

39376–39400 of 78321

CriticalFDA (Food)·F-1983-2018·2018-10-03
Zakah Life Recalls Kratom Supplements Due to Salmonella Contamination Risk
Zakah Life LLC is recalling Super Green Maeng Da Premium Kratom supplements because FDA samples tested positive for Salmonella.
Product
Super Green Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500 mg per capsules bottles, or 2) 3.52 oz // 100 grams of Kratom bags. Distributed by Zakah Life LLC Ankeny IA.
Category
Food
Distribution
4 states
CriticalFDA (Drugs)·D-0081-2019·2018-10-03
Hetero Labs Recalls Montelukast Sodium Tablets Due to Labeling Error
Hetero Labs Limited is recalling 98,016 bottles of Montelukast Sodium 10 mg tablets because one lot may contain Losartan Potassium 50 mg tablets.
Product
MONTELUKAST SODIUM — MONTELUKAST SODIUM (MONTELUKAST SODIUM)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1982-2018·2018-10-03
Zakah Life Recalls Kratom Supplements Due to Salmonella Contamination
Zakah Life LLC is recalling specific batches of Powerful Red Vein Bali Premium Kratom supplements because FDA testing found potential Salmonella contamination.
Product
Powerful Red Vein Bali Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500 mg per capsules bottles, or 2) 3.52 oz // 100 grams of Kratom bags. Distributed by Zakah Life LLC Ankeny IA.
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-3255-2018·2018-10-03
Boston Scientific Recalls ESSENTIO Pacemakers Due to Battery Depletion
Boston Scientific is recalling ESSENTIO pacemakers and CRT-P systems due to an elevated potential for early replacement caused by hydrogen-induced accelerated battery depletion.
Product
ESSENTIO Pacemaker
Category
Medical Device
Distribution
48 states
SevereFDA (Food)·F-1984-2018·2018-10-03
Zakah Life Recalls Kratom Supplements Due to Salmonella Contamination Risk
Zakah Life LLC is recalling Top Shelf White Maeng Da Premium Kratom supplements because the ingredient lacks safety assurance and red/green strains are potentially contaminated with Salmonella.
Product
Top Shelf White Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500 mg per capsules bottles, or 2) 3.52 oz // 100 grams of Kratom bags. Distributed by Zakah Life LLC Ankeny IA.
Category
Food
Distribution
4 states
SevereFDA (Food)·F-1972-2018·2018-10-03
Men's Health Supplement Recalled for Undeclared Ingredients
Confidence Inc. is recalling For-Men-10 dietary supplements because they contain undeclared ingredients, including HPMC and artificial colors.
Product
FP0392, For-Men-10, All Natural Formula to Overall Men's Health, A Dietary Supplement, 60 Tablets, UPC: 8 92483 00139 7
Category
Food
Distribution
20 states
SevereFDA (Food)·F-1985-2018·2018-10-03
Swanson Himalayan Crystal Salt Recalled for Metal Wire Contamination
Swanson Health Products is recalling Himalayan Crystal Salt because it may contain metal wire pieces. The product was distributed nationwide and in Canada and Switzerland.
Product
Swanson Ultra, Himalayan Crystal Salt, #SWU403, Net Wt. 35.27 oz. (2.2 lbs) (1,000 grams). Product of Pakistan. Distributed by Swanson Health Products, Fargo, ND 58104.
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·18V692000·2018-10-03
MCI Recalls 2018-2019 J4500 Motorcoaches for Emergency Exit Window Defect
Motor Coach Industries is recalling 2018-2019 MCI J4500 motorcoaches with 60-passenger seating due to insufficient emergency egress windows, which may delay passenger exit during an emergency.
Product
MCI — MCI J4500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1209-2018·2018-10-03
Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defect
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Product
MINIVELLE — MINIVELLE (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3257-2018·2018-10-03
Boston Scientific Recalls ACCOLADE Pacemakers Due to Battery Depletion Risk
Boston Scientific is recalling specific ACCOLADE pacemakers and CRT-P systems due to an elevated potential for early replacement caused by hydrogen-induced accelerated battery depletion.
Product
ACCOLADE Pacemaker
Category
Medical Device
Distribution
48 states
SevereFDA (Devices)·Z-3256-2018·2018-10-03
Boston Scientific Recalls PROPONENT Pacemakers Due to Battery Depletion
Boston Scientific is recalling PROPONENT pacemakers because hydrogen exposure may cause the battery to deplete faster than expected, requiring early replacement.
Product
PROPONENT Pacemaker
Category
Medical Device
Distribution
48 states
SevereFDA (Devices)·Z-3261-2018·2018-10-03
Biomet Recalls HipLOC Hip Fracture Fixation System Plates
Biomet UK Ltd. is recalling specific HipLOC hip fracture fixation system plates due to an undersized bore that prevents the lag screw from fitting.
Product
HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-130-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3245-2018·2018-10-03
Agfa DX-D 600 X-Ray System Recalled for Potential Cable Failure
Agfa N.V. is recalling 108 DX-D 600 X-ray systems because support cables may break, posing a risk of the equipment falling.
Product
DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in hospitals, clinics and medical practices by physicists, radiographers and radiologists to make, process and view static X-Ray radiographic images of the skeleton…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3279-2018·2018-10-03
GE Medical Systems Recalls Discovery MR750w MRI Systems Due to Burn Risk
GE Medical Systems is recalling 516 Discovery MR750w MRI systems because a small area on the bore surface can become warm enough to cause a serious burn if a patient touches it without proper padding.
Product
Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product Name (Model Number): A. 3.0T MR750 32CH (911000-3); B. 3.0T MR750W (5911000-3, 5481490-2, 5499460-7, 5499460-10, 5373011-3, 5352293, 5911000-3); C.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3220-2018·2018-10-03
Philips NTEGRIS Allura 9 0 FDXD Ceiling Monitor Recall
Philips is recalling NTEGRIS Allura 9 0 FDXD systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
NTEGRIS Allura 9 0 FDXD, System Code 722498 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3226-2018·2018-10-03
Philips AlIura Xper F010 F Monitor Ceiling Suspension Recall
Philips is recalling AlIura Xper F010 F systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
AlIura Xper F010 F, System Code 722002 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3278-2018·2018-10-03
CooperSurgical Retractor System Elastic Stays Recalled for Potential Seal Compromise
CooperSurgical is recalling 18,000 units of Retractor System Elastic Stays because the sterile pouch seal may be compromised, increasing the risk of infection.
Product
Retractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) Product Usage: The Retractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) are a sterile single-use medical device providing retraction to achieve and maintain optimal visualization throughout a variety…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3218-2018·2018-10-03
Philips INTEGRIS SUITE Ceiling Monitor Suspension Recall
Philips is recalling INTEGRIS SUITE systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients or users.
Product
INTEGRIS SUITE, System Code 722199 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3235-2018·2018-10-03
Philips Allura Xper F010/10 DRTable Recall for Monitor Suspension Defect
Philips is recalling 5,115 Allura Xper F010/10 DRTables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper F010/10 DRTable, System Code 722019 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19701·2018-10-03
Yamaha Recalls Golf Cars and Specialty Vehicles Due to Crash Hazard
Yamaha is recalling 145,000 golf cars and specialty vehicles because a broken accelerator pedal return spring can cause a crash.
Product
Yamaha golf cars, personal transportation and specialty vehicles
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3221-2018·2018-10-03
Philips Allura Xper FD2O Ceiling Monitor Suspension Recall
Philips is recalling 5,115 Allura Xper FD2O systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper FD2O, System Code 722006 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3229-2018·2018-10-03
Philips FlexVision Monitor Ceiling Suspension Recall for Detachment Risk
Philips is recalling FlexVision Monitor Ceiling Suspensions because the monitor may detach from the actuator rotor shaft, posing a risk of injury to patients, users, and bystanders.
Product
AIIuraXperFDlO, System Code 722010 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3248-2018·2018-10-03
Swissray Medical Recalls ddR Formula B X-ray Systems for Movement and Calibration Issues
Swissray Medical is recalling 26 ddR Formula B X-ray systems in the U.S. due to potential arm movement, calibration loss, and communication loss that could cause injury.
Product
ddR Formula B X-ray System, ddR Formula B Product Usage: X-ray system used for imaging
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3213-2018·2018-10-03
Philips INTEGRIS Allura 9 Monitor Ceiling Suspension Recall
Philips is recalling INTEGRIS Allura 9 systems because the monitor ceiling suspension may detach, causing the monitor to fall and risk injury.
Product
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3237-2018·2018-10-03
Philips Medical Monitor Ceiling Suspension Recall Due to Detachment Risk
Philips is recalling 5,115 medical monitor ceiling suspensions because the monitor may detach from the actuator rotor shaft and fall, posing a risk of injury to patients, users, and bystanders.
Product
Poly C- DMCP-Visub(H3000), System Code 72238 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide