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.
Osram is recalling specific Sealed Beam Headlamps that may not meet federal intensity requirements, potentially causing crashes due to poor visibility.
Osram Sylvania is recalling specific sealed beam headlamps that may not meet federal brightness standards, potentially reducing visibility and increasing crash risk.
The Santa Barbara Smokehouse is recalling fresh and frozen cold smoked salmon due to potential Listeria Monocytogenes contamination.
The Santa Barbara Smokehouse, Inc. is recalling Cambridge House River Run Royal Smoked Salmon due to potential Listeria Monocytogenes contamination.
The Santa Barbara Smokehouse is recalling fresh and frozen cold smoked salmon due to potential Listeria monocytogenes contamination.
The Santa Barbara Smokehouse, Inc. is recalling Cambridge House Royal Smoked Salmon due to potential Listeria monocytogenes contamination.
The Santa Barbara Smokehouse is recalling Wild River Pacific Smoked Salmon due to potential Listeria monocytogenes contamination.
The Santa Barbara Smokehouse is recalling fresh and frozen cold smoked salmon due to potential Listeria monocytogenes contamination.
The Santa Barbara Smokehouse, Inc. is recalling specific lots of smoked salmon due to potential Listeria monocytogenes contamination.
Hill-Rom is recalling Steriseal-Cannula Ophthalmic handpieces because the metal cannula can rotate and become dislodged from the plastic handpiece.
Vitamin Cottage Natural Food Markets is recalling specific lots of Natural Grocers Raw Macadamia Nuts due to potential Salmonella contamination.
Yoli, Inc. is recalling Mi Costenita Bocadin chocolate-covered wafers due to undeclared milk allergens. The product was distributed nationwide in 26 states.
Gillig is recalling 2010-2015 Low Floor transit buses because a power cable may chafe a fuel line, increasing fire risk.
General Motors is recalling specific Hummer H3 and H3T vehicles because the blower motor connector may overheat, increasing the risk of a fire.
Stryker is recalling specific Optical Access Systems because they may fracture at the tip, leaving fragments at the surgical site.
Stryker is recalling Fios First Entry trocars because some may fracture at the distal tip, leaving fragments at the surgical site.
Nissan is recalling 2013-2014 Juke, Cube, and 2014 Versa vehicles because the engine start/stop button may stick, potentially causing the engine to shut off while driving.
Stryker Endoscopy is recalling 22,063 SERFAS 90 degree Energy Probes because fragments of the probe have been reported to break off into patients during arthroscopic procedures.
The Santa Barbara Smokehouse is recalling fresh and frozen cold smoked salmon due to potential Listeria Monocytogenes contamination.
Teleflex Medical is recalling 9,333 units of Lifesaver Single Patient Use Manual Resuscitators because the intake port may be blocked, causing the bag to fail to fill.
The Santa Barbara Smokehouse is recalling approximately 250,000 pounds of Atlantic smoked salmon products due to potential Listeria monocytogenes contamination.
Stryker is recalling specific cannula and seal models because they may fracture at the tip, leaving fragments at the surgical site.
Fresenius Medical Care is recalling NaturaLyte Liquid Bicarbonate Concentrate due to bacterial contamination. The product is used in hemodialysis machines.
Otteroo is recalling about 3,000 inflatable baby floats because seams can leak air and deflate, posing a drowning risk. No injuries have been reported.
Remel Inc. is recalling 143 VersaTREK Instrument Series 240 devices because their use may result in false positive reports. The devices are used to cultivate microorganisms from blood and other sterile bodily fluids.