State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Forest River is recalling 1,497 model year 2016 trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.
Kalmar is recalling 2010-2014 Ottawa T2 tractors because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.
Pali Design is recalling approximately 18,000 children's furniture units in the U.S. because a plastic restraint strap can break, allowing the furniture to tip over and cause injury or death.
Kia is recalling 2011 Sportage vehicles because the brake light switch may fail, preventing brake lights from illuminating and increasing crash risk.
Gulf Stream is recalling 2015 Canyon Trail and Sedona trailers because entry step rivets may shear, causing steps to fail and increasing the risk of falls.
Vermeer is recalling specific 2015 TLR30HD and TLR30LD trailers because an incorrectly installed safety chain may fail to prevent the trailer from separating from the tow vehicle.
Mercedes-Benz is recalling specific 2015 E250, GLK250, and ML250 vehicles because oil may leak from the chain tensioner gasket, creating a fire hazard.
Fontaine is recalling 2016 Revolution semi-trailers because hardened washers may crack, potentially causing structural detachment and increasing crash risk.
Prevost is recalling 314 X3-45 coaches from 2006-2010 because rusted booster studs may break, allowing power cables to short against the frame and cause a fire.
Prevost is recalling 2015 X3-45 and H3-45 coaches because front suspension bolts may fail, potentially causing loss of vehicle control.
Nova Bus is recalling 250 model year 2001-2004 LFS buses because incorrectly connected air hoses may delay parking brake application, increasing crash risk.
Prevost is recalling 452 model year 2010-2014 coaches because engine heat may damage fire suppression wires, potentially causing an engine shutdown and crash.
Bariatric Fusion is recalling cherry-flavored iron soft chews because the packaging fails to meet child-resistant closure requirements, posing a risk to young children.
Quincy Street, Inc. is recalling approximately 49,308 pounds of pork sausage products that may be contaminated with foreign materials. The products were shipped to institutions nationwide.
Cree Inc. is recalling approximately 700,000 LED T8 replacement lamps sold in the U.S. because electrical arcing can cause the lamps to overheat and melt, posing a burn hazard.
Big Lots is recalling about 16,000 hanging chairs because they can tip over and cause falls. Consumers should stop using them and return the base for a refund.
Hospira is recalling 24,744 bags of Lactated Ringer's Irrigation due to confirmed mold contamination. The product was distributed nationwide.
Strohecker's Pharmacy is recalling 365 vials of Testosterone Cypionate 200 mg/mL because they contain Estradiol Valerate 20 mg/mL instead.
Advanced Physician Solutions is recalling 17 vials of Estradiol Valerate Injectable because the FDA determined there is a lack of assurance of sterility.
Advanced Physician Solutions, Inc. is recalling Hydroxyzine Hydrochloride Injectable because the product lacks assurance of sterility. The recall covers 3 vials distributed nationwide.
Advanced Physician Solutions, Inc. is recalling Sodium Tetradecyl Sulfate (Sterile Water) 3.5% Injectable due to a lack of assurance of sterility.
Advanced Physician Solutions is recalling Estradiol Valerate Injectable because the product lacks assurance of sterility.
Advanced Physician Solutions is recalling Sodium Tetradecyl Injectable vials nationwide because the company cannot ensure the product is sterile.
Advanced Physician Solutions, Inc. is recalling injectable glutathione vials because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Advanced Physician Solutions is recalling 21 vials of Sodium Hyaluronate Injectable due to a lack of assurance of sterility. The product was distributed nationwide.