State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Thor Motor Coach is recalling 2017 Outlaw motorhomes because a warning label near the fuel fill station is missing, which could increase the risk of fire if an operator smokes.
NatureBox is recalling Country Ranch Sunflower Kernels due to a supplier notification regarding Listeria monocytogenes. The product was sold nationwide online.
NatureBox is recalling Cheddar and Onion Sunflower Kernels due to a supplier notification regarding Listeria Monocytogenes contamination.
Dakota Style, Inc. is recalling Savory Bacon Sunflower Kernels because they may be contaminated with Listeria monocytogenes.
NatureBox, Inc. is recalling SunOpta Country Ranch Sunflower Kernels due to a supplier notification regarding Listeria Monocytogenes contamination.
Dakota Style, Inc. is recalling Roasted & Salted Sunflower Kernels because they may be contaminated with Listeria monocytogenes.
Let's Talk Health is recalling 75 units of Tox Elim Liquid due to undeclared whey protein and soy lecithin, posing a risk to individuals with milk or soy allergies.
Let's Talk Health, Inc. is recalling Energizer Drink Mix Citrus because it contains undeclared whey protein (milk) and soy lecithin.
Let's Talk Health, Inc. is recalling specific lots of Pomegranate Energizer Drink Mix due to undeclared whey protein, which contains milk and soy lecithin.
Transcraft is recalling 2015-2017 Platform Trailers because improperly machined spring brake valves may delay braking, causing the trailer to roll away.
Let's Talk Health is recalling 200 units of Agua Vitae Kids Multi-Vitamin Liquid due to undeclared whey protein and soy lecithin.
Let's Talk Health, Inc. is recalling Aqua Vitae Multi-Vitamin due to undeclared whey protein and soy lecithin.
Let's Talk Health, Inc. is recalling specific lots of Energizer Drink Mix because they contain undeclared milk and soy.
Ford is recalling 2016 Transit Connect vehicles because metallic debris in the brake pump may degrade electronic stability control, increasing crash risk.
Wabash National is recalling 2015-2017 Van Trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Nissan is recalling 1,522 model year 2016 Sentra vehicles because an engine room harness terminal pin may be too large, potentially causing the engine to stall or fail to start.
Newmar is recalling 2017 Ventana and Dutch Star motorhomes because wipers may block the view or headlights may turn off, increasing crash risk.
Ceg Enterprises is recalling Germ Terminator GT100 toothbrush sanitizers due to reports of excessive heat, power cord discoloration, and suspected counterfeit UL labels.
Saro Trading is recalling about 7,800 children's nightgowns because they fail to meet federal flammability standards, posing a risk of burn injuries.
Immuno-Mycologics, Inc. is recalling 467 units of Histoplasma Yeast Complement Fixation Antigen Dilute (Lot 111WH3) due to bacterial contamination. The product was distributed nationwide to specific states.
Siemens Medical Solutions is recalling 2 Biograph TruePoint scanner upgrades because using non-Siemens phantoms for calibration may result in unexpected SUV values.
Fresenius Medical Care is recalling 875 CLiC monitors used with 2008T hemodialysis machines because a frozen screen may cause the blood pump to stop.
Siemens is recalling 83 Biograph mCT-X 4R scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.
Kia is recalling 2016 Sorento vehicles because a rear suspension component may not be properly welded, which could break and increase the risk of a crash.
Fujifilm Medical Systems is recalling 27 units of Synapse PACS software versions 4.4.000 through 4.4.020 because the software fails to display medical images, showing an error message instead.