State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
E-Z-GO is recalling about 8,200 gas-powered golf, shuttle, and utility vehicles because the gas tank can leak, posing a fire hazard.
Hyundai is recalling 2015 Sonata vehicles because the front passenger seat belt buckle may prevent fastening, increasing injury risk in a crash.
General Motors is recalling 2007-2012 Buick Enclave, Chevrolet Traverse, GMC Acadia, and Saturn Outlook vehicles because power liftgate gas struts may wear prematurely, causing the liftgate to fall suddenly.
Technosport is recalling Omersub Zero Cube scuba masks because non-conforming glass lenses can shatter during normal use, posing an injury hazard.
Yamaha is recalling 2008-2015 WR250X and WR250R motorcycles because a stator coil defect may cause the battery to die and the engine to stall, increasing crash risk.
Carson is recalling 2009-2012 Fun Runner trailers because a door lock defect may jam the deadbolt, trapping occupants inside.
Keystone is recalling 2013 Montana and 2014 Mountaineer trailers because rear windows are incorrectly labeled as emergency exits or blocked by ladders, potentially delaying escape.
OFT Inc is recalling approximately 67,232 pounds of beef leg bone extract and beef concentrate products produced in Australia and New Zealand that were not presented for U.S. import inspection.
Northern Tool + Equipment is recalling Little Digger Toys because the red paint contains excessive lead levels prohibited by federal law.
lululemon athletica is recalling about 133,000 women's tops in the U.S. because elastic draw cords can snap back and injure the face or eyes.
AstraZeneca is recalling NEXIUM capsules because a retail pharmacist found SEROQUEL XR tablets in an unopened bottle.
Shred-Tech is recalling specific MDS models because EPA emission controls cause the front axle to exceed its certified weight rating, increasing crash risk.
Cruiser RV is recalling 2016 Stryker travel trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.
SR Suntour is recalling bicycles with specific fork models because a bolt can break, causing the front wheel to detach. This poses a crash hazard to riders.
Beaver-Visitec International is recalling 621 ophthalmic procedure kits because the included Devon Light Glove may have holes or slits that compromise sterility.
Positec Tool Corp. is recalling Worx electric blower/vacs because reversed wiring poses a shock hazard. No injuries have been reported.
Stryker is recalling 72 Navigation System II-Carts because a weld seam defect may cause the articulated arm joint to fail.
Beaver-Visitec International Inc. is recalling 268 ophthalmic procedure kits because the included Devon Light Gloves may have holes or slits that compromise sterility.
Smiths Medical is recalling CADD-Solis Ambulatory Infusion Pumps because the locking assembly may bind, preventing the cassette or keypad from locking securely.
Beaver-Visitec International is recalling 585 ophthalmic procedure kits because the Devon Light Glove component may have holes or slits that compromise sterility.
Synthes, Inc. is recalling Pull Reduction Devices for 4.3mm Percutaneous Drill Guides because incorrect hardness specifications may cause the devices to break during surgery.
Integra LifeSciences is recalling Camino Intracranial Pressure Monitoring Catheters because incorrect assembly may allow cerebrospinal fluid or blood to leak.
Mortara Instrument is recalling 176 ELI 380 electrocardiographs because ECG waveforms may be incorrectly associated with the wrong patient's demographics when transmitted to records systems.
CareFusion 303, Inc. is recalling 63 Alaris PC unit model 8015 infusion pumps due to a software defect that may allow infusions to start outside hospital-established limits.
Beaver-Visitec is recalling 384 ophthalmic procedure kits because the included Devon Light Gloves may have holes or slits that compromise sterility.