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.
Elgin is recalling 2014 Eagle and Road Wizard street sweepers because battery and alternator wiring may conduct excessive current, increasing the risk of a fire.
Suzuki is recalling 2010-2013 Kizashi and SX4 vehicles because the shift selector can move out of Park without the brake pedal being depressed, increasing crash risk.
Navistar is recalling 2013-2015 International WorkStar trucks because reversed headlight wiring may reduce light output, increasing crash risk.
James Trading Group is recalling Croker Kids GAA Fleece Panel Hoodies because the neck drawstrings pose a strangulation hazard to children.
Roadhouse Distribution is recalling Voss 888CF motorcycle helmets because the shell material failed penetration testing, increasing injury risk in crashes.
Shark is recalling specific RAW motorcycle helmets that failed federal impact attenuation tests, increasing the risk of injury in a crash.
ZF Group is recalling 9-speed automatic transmissions where a contaminated parking pawl may dislodge, preventing the vehicle from locking in Park and increasing crash risk.
Nissan is recalling 2015 Armada vehicles because a transmission defect may prevent the parking pawl from fully engaging, allowing the vehicle to move while in Park.
Comfort Research is recalling about 125,000 vinyl bean bag chairs because zippers can be opened by children, posing a risk of entrapment and suffocation.
ARBOC is recalling 2015 Spirit of Mobility and Freedom buses because exterior electrical connections may not be weatherized, increasing fire risk.
General Motors is recalling 2015 Cadillac SRX vehicles because the front driver's seat track bracket may be incorrect, potentially causing the seat to detach during a crash.
BRP is recalling Ski-Doo and Can-Am kids' hoodies because the neck drawstrings pose a strangulation hazard. No injuries have been reported.
Katadyn North America Foods is recalling 2,719 pounds of Spicy Sausage Pasta because the label lists beef but the product contains pork.
Yamaha is recalling about 875 model year 2015 YZ250FFL and YZ250FFW competition off-road motorcycles because the engine can lock up during operation, causing a crash.
Kiddie Korral is recalling pink hooded sweatshirts for children because the drawstrings pose a strangulation risk. Consumers should remove the drawstrings or return the items for a refund.
Giggles International is recalling about 13,000 Animated Sing-Along Monkey toys sold at Cracker Barrel because the battery compartment can overheat and cause burns.
Schneider Electric is recalling about 62,500 PowerPact J-frame circuit breakers because they may fail to trip during overloads, posing fire, burn, and shock risks.
Fresenius Kabi USA is recalling 101,200 vials of Midazolam Hydrochloride Injection due to potential glass fractures and particles that compromise sterility.
Nellcor Puritan Bennett is recalling 324 Puritan Bennett 980 Ventilators because a capacitor component can fail, causing a dim screen and thermal odor.
Fresenius Kabi USA is recalling 184,550 vials of Ondansetron Injection due to potential glass fractures and particles that compromise sterility.
TomoTherapy Incorporated is recalling 210 TomoTherapy Treatment Systems worldwide due to a software defect that may fail to monitor jaw position after an error, potentially leading to incorrect treatment delivery.
Ferrara is recalling 12 model year 2014 Fire Custom trucks because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
PFM Medical is recalling ASEPT 600 ml Drainage Kits because they may exceed USP limits for bacterial endotoxin. The recall affects 1,470 units distributed in the US and abroad.
Fresenius Kabi USA is recalling 240,550 vials of Cyanocobalamin Injection due to potential glass fractures and particles that compromise sterility.
Siemens is recalling three Mammomat Inspiration systems because the workstation table may fall over if not secured, posing a risk of serious injury.