State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
High Liner Foods is recalling Schwan's Haddock Sticks because the product may contain undeclared milk, posing a risk to individuals with milk allergies.
High Liner Foods is recalling Sea Cuisine Pan Sear Teriyaki Salmon because it may contain undeclared milk. This poses a risk to consumers with milk allergies.
High Liner Foods is recalling Sea Queen Fish Sticks because they may contain undeclared milk, posing a risk to consumers with milk allergies.
High Liner Foods Inc. is recalling specific lots of breaded Alaska pollock squares because they may contain undeclared milk.
High Liner Foods Inc. is recalling Hain-Celestial Earth's Best Fish Nuggets because the product may contain undeclared milk.
High Liner Foods Inc. is recalling specific lots of breaded Alaska Pollock FishFries because the product may contain undeclared milk.
High Liner Foods Inc. is recalling specific lots of Guinness Battered Cod Fillets because they may contain undeclared milk, a major food allergen.
Akorn Inc is recalling Chlorhexidine Gluconate Oral Rinse unit dose cups because crystallization caused subpotent assay results.
AvKARE Inc. is recalling specific lots of Voriconazole Tablets, 200 mg, because they failed impurity specifications for a related compound.
Akorn Inc is recalling Halyard 24-Hour Oral Care Kits containing chlorhexidine gluconate oral rinse due to crystallization and subpotent assay results.
KVK-Tech, Inc. is recalling specific lots of Phentermine Hydrochloride capsules because they failed impurity specifications during stability testing.
Akorn Inc is recalling Halyard 24-Hour Oral Care Kits containing chlorhexidine gluconate oral rinse due to crystallization and subpotent assay results.
General Motors is recalling 2017-2018 GMC Acadia, 2018 Chevrolet Equinox, and 2018 GMC Terrain vehicles because the right front intermediate driveshaft may fracture and separate while driving.
Polaris is recalling about 1,600 2017 GENERAL Base and Hunter recreational off-highway vehicles because inconsistent tire pressure information can lead to improperly inflated tires and a crash hazard.
BMW is recalling specific motorcycles because accessory turn signals may be insufficiently visible to other drivers, increasing crash risk.
Iowa Mold Tooling is recalling 2016-2017 Dominator Contractor trucks because a fuse block may contact the hood, creating an electrical short that increases fire risk.
Command Electronics is recalling specific LED ceiling lights installed in Jayco and Highland Ridge recreational vehicles because they may produce excessive heat, increasing the risk of a fire.
Heartland is recalling 2018 Pioneer recreational trailers because the liquid propane hose may not be secured, allowing the tire to rub through it and cause a leak.
Forest River is recalling 2018 Prime Time recreational trailers because the Federal Placard lists an incorrect Gross Axle Weight Rating, which could lead to axle failure.
Forest River is recalling 2018 Dynamax, Forester, Sunseeker, and Coachmen Prism vehicles because B-pillar tire labels list pressures that are too low.
Blue Bird is recalling 2015-2019 Vision and 2016 All American school buses because unpadded seat studs may cause head injuries in rear crashes.
Tiny Idahomes is recalling 2014-2017 RVs and trailers because the Federal Placard may display an incorrect Gross Vehicle Weight Rating (GVWR). Owners will receive corrected labels by mail.
Cook Medical is recalling Zenith Alpha Thoracic Endovascular Grafts due to reports of graft thrombosis and occlusion, including one patient death.
Cantrell Drug Company is recalling 21,080 syringes of Glycopyrrolate Injection Solution due to a lack of sterility assurance.
Cantrell Drug Company is recalling Diltiazem HCl 125 mg in 5% Dextrose single-dose bags because of a lack of sterility assurance. The recall covers 2,761 bags distributed nationwide.