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.
Carli Suspension is recalling adjustable track bars for specific Ram trucks because a joint may break, causing loss of steering and increasing crash risk.
Vantage Mobility International is recalling 2017 Chrysler Pacifica lowered floor vehicles because rear pinion brackets may crack, causing wheel wobble and potential loss of control.
Daimler Vans USA is recalling 2010-2011 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture during deployment.
Dana is recalling Spicer D-Series and E-Series steer axles because the castellated nut may not be properly torqued, allowing the tie rod to loosen and potentially disconnect.
Daimler Vans USA is recalling 2012 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because the passenger air bag inflators may rupture during deployment, posing a risk of serious injury or death.
Nestlé Waters is recalling about 12,300 AccuPure floor-standing filtration dispensers because they can overheat, smoke, or catch fire. No injuries have been reported.
Daimler Vans USA is recalling 2007-2009 Dodge and Freightliner Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture in a crash.
BMW is recalling specific motorcycles because optional aluminum luggage cases may block rear reflex reflectors, increasing crash risk.
Nissan is recalling 2016-2018 Infiniti Q50 and 2017 Q60 vehicles with 2.0L engines because faulty fuel pump software may cause the engine to stall while driving.
Really Good Stuff is recalling Write Again magnetic dry erase boards because the metal surface can separate, posing a laceration hazard.
REV Recreation Group is recalling 219 motorhomes because headlights may lack tempered glass lenses, which could crack and reduce visibility.
Flowonix Medical is recalling Prometra II implantable infusion pumps after a report of a fatal drug overdose during an MRI procedure.
Penumbra Inc. is recalling 155 units of the 3D Revascularization Device because a raw material issue could cause the delivery wire to break, potentially leading to serious injury or death.
New England Natural Bakers is recalling Aldi Millville Fruit & Nut Whole Grain Granola due to potential Listeria monocytogenes contamination.
New England Natural Bakers is recalling Evoke Organic Muesli Classic Swiss 12 oz. pouches due to potential Listeria monocytogenes contamination.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
Mazda is recalling specific 2003-2008 models because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Becton Dickinson is recalling 648,000 units of BD 3ml Syringes because several lots did not receive the specified dose of irradiation required to meet the Sterility Assurance Level.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection because a media fill failure at the manufacturer raised concerns about sterility.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
Becton Dickinson is recalling 547,600 units of BD 10mL Syringes because several lots did not receive the specified dose of irradiation required to meet Sterility Assurance Level standards.
PharMedium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.
PharMEDium Services is recalling specific lots of Potassium Phosphate Injection due to a media fill failure that compromised sterility assurance.