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.

37676–37700 of 78321

HighFDA (Devices)·Z-0852-2019·2019-02-27
Boston Scientific Recalls Mislabelled Stingray Guidewires for Coronary Procedures
Boston Scientific is recalling 49 Stingray Guidewires that are 185cm but incorrectly labeled as 300cm. The mislabeling could lead to improper use during angioplasty procedures.
Product
Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0513-2019·2019-02-27
Lupin Recalls Lovastatin Tablets Due to CGMP Deviations
Lupin Pharmaceuticals is recalling Lovastatin 40 mg tablets because the drug substance used was out of specification for impurity results.
Product
LOVASTATIN — LOVASTATIN (LOVASTATIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0844-2019·2019-02-27
Ortho Vitros Myoglobin Calibrators Recalled for Stability Issues
Ortho Clinical Diagnostics is recalling Vitros Myoglobin Calibrators due to a stability issue that may cause calibration failures or atypical quality control results.
Product
Vitros Myoglobin Calibrators, Product Code 6801043 For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System for the quantitative measurement of myoglobin in human serum and plasma
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0499-2019·2019-02-27
Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotency
Advanced Pharma Inc. is recalling Oxytocin 30 Units Injectable Solution because the product may contain higher concentrations than labeled.
Product
Oxytocin 30 Units added to NS 500 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 503 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-706-50.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0511-2019·2019-02-27
Akorn Recalls Moisturizing Lubricant Eye Drops Due to Stability Failure
Akorn Inc is recalling specific lots of Moisturizing Lubricant Eye Drops because they failed stability specifications for Sodium Perborate.
Product
Moisturizing Lubricant Eye Drops, 0.25% Sodium Carboxymethylcellulose, 0.5 Fl OZ (15mL) Distributed by: Walgreen Co, 200 Wilmont Rd Deerfield IL 60015 NDC 00363-9651-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0842-2019·2019-02-27
Smiths Medical Recalls Arterial Blood Sampling Kits with Povidone Iodine Pads
Smiths Medical ASD Inc. is recalling arterial blood sampling kits because the included povidone iodine prep pads may not maintain potency through their expiration dates.
Product
Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, models 4589P-1, 4591EG-1, 4591P-1, 4599P-1, 4611LH, 4611P-1, 4620EG-1, 4620P-1, 4640LH, 4640P-1, 4649P-1, 4660EG-1, 4660P-1…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0515-2019·2019-02-27
Akorn Recalls Clobetasol Propionate Cream Due to Preservative Stability Failure
Akorn Inc. is recalling specific lots of Clobetasol Propionate Emollient Cream 0.05% because stability testing revealed out-of-specification preservative levels.
Product
Clobetasol Propionate Emollient Cream 0.05%, a) 30 gram (NDC 50383-270-30) and b) 60 gram (NDC 50383-270-60) tubes, Rx only. Manufacturer: Akorn Inc. 369 Bayview Ave., Amityville, NY 117701.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0498-2019·2019-02-27
Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotency
Advanced Pharma Inc. is recalling 672 bags of Oxytocin 20 Units Injectable Solution because the product may contain higher concentrations than labeled.
Product
Oxytocin 20 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1002 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-703-99.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0843-2019·2019-02-27
Smiths Medical Recalls Arterial Blood Sampling Kits Due to Iodine Potency
Smiths Medical ASD Inc. is recalling Portex Pulsator Arterial Blood Sampling Kits because the included povidone iodine prep pads may not maintain potency through their expiration dates.
Product
Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial Blood Sampling Kit with Liquid Sodium Heparin, models 4037NP-1, 4039-1, 4039EG-1, 4044EG-1, 4044P-1, 4057NP-1, 4067NP-1, 4077EG-1, 4077NP-1, 4084P-1, G1193, G1374, G1585, G1589, G1598, G1621, and G1806.…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0512-2019·2019-02-27
Perrigo Recalls Ciclopirox Shampoo Due to Stability Testing Failures
Perrigo New York, Inc. is recalling specific lots of Ciclopirox shampoo 1% because stability testing revealed out-of-specification related substances.
Product
CICLOPIROX — CICLOPIROX (CICLOPIROX)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0497-2019·2019-02-27
Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotent Drug Concerns
Advanced Pharma Inc. is recalling 12 bags of Oxytocin 10 Units Injectable Solution because the product may contain higher concentrations than labeled.
Product
Oxytocin 10 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1001 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-730-99.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0514-2019·2019-02-27
Mometasone Furoate Cream Recalled for NDC Typographical Error
ACP Nimble Buyer, Inc. is recalling Mometasone Furoate Cream due to a typographical error in the National Drug Code (NDC) on the label.
Product
Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories, Inc. South Plainfield, NJ 07080, NDC 0713-0726-37
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V122000·2019-02-26
International LT and Prostar Trucks Recalled for Exhaust Bracket Crack Risk
Navistar is recalling 2016-2020 International LT and 2017-2018 Prostar trucks because a cracked exhaust bracket could cause the tailpipe to detach, creating a road hazard.
Product
INTERNATIONAL — INTERNATIONAL PROSTAR, LT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V132000·2019-02-26
Mercedes-Benz Recalls GLA 250 Vehicles for Rear Seat Covering Defect
Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because an incorrect rear seat covering may hide the center child seat anchor point, increasing crash injury risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLA 250
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V131000·2019-02-26
Mercedes-Benz Recalls 2018 CLA 250 Vehicles for Tail Light Defect
Mercedes-Benz is recalling 2018 CLA 250 and CLA 250 4MATIC vehicles because tail and side marker lights may flicker or fail, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ CLA 250
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V130000·2019-02-26
Mercedes-Benz Recalls C and E Class Vehicles for Seatback Lock Defect
Mercedes-Benz is recalling 2017-2018 C and E Class vehicles because front seatbacks may not lock properly, increasing injury risk in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ C 300, E 400, AMG C43, AMG C63
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19071·2019-02-26
JumpSport Recalls Mini Trampolines Due to Frame Injury Hazard
JumpSport is recalling about 11,300 half-fold fitness mini-trampolines because the folding frame can forcefully hit users, causing cuts, bruises, and dental injuries.
Product
JumpSport® half-fold fitness mini-trampolines
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·19V129000·2019-02-26
Keystone Recalls 2018-2019 Recreational Trailers Due to Cargo Tray Rivet Failure
Keystone RV is recalling certain 2018-2019 recreational trailers because cargo tray rivets may shear, allowing the tray to detach and potentially injure someone.
Product
KEYSTONE — KEYSTONE MONTANA HIGH COUNTRY, MONTANA, AVALANCHE, ALPINE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V125000·2019-02-26
Ford E-250 wheelchair lift cam failure recall
New England Wheels is recalling 2008, 2013, and 2014 Ford E-250 vans with Ricon wheelchair lifts because the positioning cam may fail, causing the platform to rise too high.
Product
FORD — FORD E-250
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19072·2019-02-26
D&D Futon Furniture Recalls Folding Foam Beds for Fire Hazard
D&D Futon Furniture is recalling about 800 Sleeper Chair Folding Foam Beds because they fail to meet federal flammability standards, posing a fire hazard.
Product
Sleeper Chair Folding Foam Beds
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·19V128000·2019-02-26
Foundation Ambulance Recalls 2017-2018 Type I and III Vehicles for Brake Light Defect
Foundation Ambulance is recalling 2017-2018 Type I and III ambulances because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.
Product
FOUNDATION AMBULANCE — FOUNDATION AMBULANCE TYPE I AMBULANCE, TYPE III AMBULANCE
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·19E016000·2019-02-25
Takata Driver Air Bag Inflator Recall for Rupture Risk
Takata is recalling certain driver frontal air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.
Product
AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V123000·2019-02-25
Jayco Recalls 2019 Embark Motorhomes Due to Brake Component Defect
Jayco is recalling 2019 Embark motorhomes because missing or improperly installed cotter pins may cause brake actuator rods to detach, increasing stopping distance and crash risk.
Product
JAYCO — JAYCO EMBARK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19E015000·2019-02-25
Meritor Recalls EX225 Disc Brake Calipers Due to Cracked Drive Pins
Meritor is recalling specific EX225 disc brake calipers because cracked drive pins may fracture, causing the vehicle to pull to one side while braking and increasing crash risk.
Product
SERVICE BRAKES, AIR:DISC:CALIPER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V124000·2019-02-25
Entegra Reatta Motorhomes Recalled for Front Brake Defect
Entegra is recalling 2019 Reatta motorhomes because missing or improper cotter pins on front brakes may reduce stopping power and increase crash risk.
Product
ENTEGRA — ENTEGRA REATTA
Category
Vehicle
Distribution
Distributed nationwide