State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Triple E is recalling 2017-2018 Unity, Wonder, and Serenity motorhomes because incorrect labels may indicate higher cargo capacity than actual, increasing crash risk.
Goodman Manufacturing is recalling about 1,650 modular blowers in the U.S. because incorrect electrical information on the serial plate could lead to fire hazards.
Olli Salumeria Americana is recalling approximately 3,946 pounds of ready-to-eat meat products that may be contaminated with Listeria monocytogenes.
Keystone is recalling 2,958 specific 2018 recreational trailers because a loose propane valve screw may cause gas leaks and fire.
Newmar is recalling 2018 Essex motorhomes because taillights may loosen and detach while driving, increasing crash risk. Dealers will secure the lights with new hardware.
Double Insight is recalling Gem 65 8-in-1 multicookers sold at Walmart because a defect can cause the unit to overheat and melt, posing a fire hazard.
Jaguar is recalling 2018 E-Pace vehicles because improperly installed front brake hose brackets may allow hoses to contact tires, causing fluid leaks and increased stopping distances.
Goodman is recalling about 534,000 packaged terminal air conditioners in the U.S. because outdoor fan motors can overheat, posing fire and burn risks.
Graco is recalling about 36,000 Table2Table 6-in-1 highchairs sold at Walmart because the rear legs can pivot out of position, creating a fall hazard.
Coach House is recalling 2003-2018 recreational vehicles equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks during a fire.
Ford is recalling 2017-2018 Taurus vehicles because the ignition key may be removed when the transmission is not in Park, increasing the risk of the vehicle rolling away.
Jaguar Land Rover is recalling 2018 Range Rover Velar vehicles because ventilation system parts may detach, preventing fog removal from windows and increasing crash risk.
RockyMounts is recalling four bicycle rack models because a weld may crack, causing the rack and bicycles to separate from the vehicle and create a road hazard.
Medtronic is recalling 951 Compia MRI CRT-Ds because a defect may prevent the delivery of high and low voltage therapy.
Medtronic is recalling 951 Evera ICDs and CRT-Ds because a defect may prevent the devices from delivering high or low voltage therapy.
Pharmedium Services, LLC is recalling all lots of Neostigmine Methylsulfate Injection due to a lack of sterility assurance.
Allen Medical Systems is recalling 161 Radiolucent Surgery Spine Frames because the base may crack during patient transfer.
Pharmedium Services, LLC is recalling all lots of Ropivacaine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.
Pharmedium Services, LLC is recalling all lots of Adenosine Injection because of a lack of sterility assurance. The recall covers products distributed nationwide.
Pharmedium Services, LLC is recalling Meperidine HCl in 0.9% Sodium Chloride injections nationwide due to a lack of sterility assurance.
Pharmedium Services, LLC is recalling all lots of Ketamine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.
Pharmedium Services, LLC is recalling Methadone HCl Injection in all strengths and packaging due to a lack of sterility assurance.
Pharmedium Services, LLC is recalling Labetalol HCl in 0.9% Sodium Chloride infusions nationwide due to a lack of sterility assurance.
Medtronic is recalling 951 Amplia MRI CRT-D devices because they may fail to deliver high or low voltage therapy.
Medtronic is recalling 951 Visia AF MRI ICDs and CRT-Ds because a defect may prevent high and low voltage therapy.