State
73,738 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.
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.
Fenton Mobility is recalling 2015-2018 Ford Transit vehicles equipped with specific foldaway seats that may fail to lock in place during a crash, increasing injury risk.
FCA US is recalling 2018-2019 Ram 1500 trucks because an incomplete weld on the rear driveshaft may crack or fracture, creating a road hazard or loss of drive power.
General Motors is recalling specific 2017-2019 Chevrolet Silverado and GMC Sierra trucks because a short circuit in the engine block heater could cause a fire.
Mazda is recalling 2011-2013 Mazda6 vehicles sold or registered in specific states because the front cross member may corrode, potentially affecting steering alignment.
Volvo is recalling 2019 S60 vehicles because rear suspension lock nuts may not be properly tightened, which could cause sudden handling changes and increase crash risk.
Viessmann is recalling Vitodens 200-W and 222-F boilers because a corroded heat exchanger can leak flue gases, posing a carbon monoxide poisoning hazard.
Jaguar is recalling 2014-2015 F-TYPE vehicles because a seatbelt sensor wiring error may cause the front passenger air bag to deploy incorrectly, increasing injury risk for children.
TriDerma is recalling Pain Relief Cream with Lidocaine because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk to young children.
Ruggable is recalling about 6,200 shag area rugs because the shag covers fail to meet federal flammability standards, posing a fire hazard.
Little Red Rooster Company is recalling NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert because it contains undeclared almonds.
The FDA is recalling Kopi Jantan Tradisional Natural Herbs Coffee because it contains undeclared sildenafil and tadalafil, unapproved drugs for erectile dysfunction.
Anderson Compounding Pharmacy is recalling Serum Tears 50% Ophthalmic Drops due to a lack of sterility assurance. All lots are affected nationwide.
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix 30:30:1 Injection vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Methylcobalamin 3000 mcg/mL Injection Solution due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Neomycin 40 mg/Polymixin B 200,000 Bladder Irrigation Solution due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix 50:30:1 vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling 23 vials of Prostaglandin 20 mcg/mL due to a lack of sterility assurance. The product was distributed nationwide.
Anderson Compounding Pharmacy is recalling HCG 20 Day Injection vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Testosterone Cypionate 250 mg/mL sterile injections because the product lacks sterility assurance.
Brainlab AG is recalling Spine & Trauma 3D Navigation 1.0 software because it may display fixed image planes instead of the desired inline view, potentially preventing surgeons from determining instrument position.
ICU Medical is recalling specific lots of ChemoClave Vented Vial Spikes because they may contain plastic burr particulate from the protective cap.
Anderson Compounding Pharmacy is recalling specific 60 mL syringes containing Heparin, Marcain, Sodium Bicarbonate, and Normal Saline due to a lack of sterility assurance.
ICU Medical is recalling specific lots of ChemoClave Vial Spikes because they may contain plastic burr particulate from the protective cap.
Anderson Compounding Pharmacy is recalling 12 syringes of a Heparin, Marcain, and Sodium Bicarbonate mixture due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Heparin and Marcaine syringes due to a lack of sterility assurance. The recall covers all lots distributed nationwide.