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.
Nissan is recalling 46,846 Altima and Maxima vehicles because an improperly installed o-ring may cause fuel to leak during a crash, increasing fire risk.
Volkswagen is recalling specific 2010-2014 models because debris may damage the air bag clock spring, preventing the driver's air bag from deploying in a crash.
John Deere is recalling specific riding lawn tractors because a brake arm can fail, posing a crash hazard that could result in serious injury or death.
Forest River is recalling 2015-2016 Cedar Creek Silver Back recreational vehicles because the gross vehicle weight rating on the certification label is incorrect.
Manhattan Group is recalling My Snuggly Ellie Activity Toys because the wooden ring can break into small pieces, posing a choking hazard to young children.
Good Food Made Simple is recalling approximately 3,574 pounds of turkey and pork breakfast products that were distributed in California without U.S. inspection.
NVIDIA is recalling approximately 83,000 SHIELD tablet computers because the lithium-ion batteries can overheat and pose a fire hazard.
USDA FSIS issued a public health alert for whole pigs used for roasts due to possible Salmonella contamination linked to illness clusters in Washington.
Temsa is recalling 2013-2016 TS45 coaches because low air pressure may cause parking brakes to drag, overheat, and potentially start a fire.
Stork Craft is recalling about 18,500 foam crib mattresses because they fail to meet federal flammability standards, posing a fire hazard.
Nipponflex is recalling about 400 Smart Flex and Smart Care mattresses because they fail to meet federal flammability standards, posing a fire hazard.
Forest River is recalling 160 motorhomes because the back-up camera system may display reversed images, increasing the risk of a crash.
Liftmoore is recalling 2001-2006 6036WX truck cranes because a specific battery equalizer part may conduct electricity when heated, increasing fire risk.
Forest River is recalling 2014-2016 Sandpiper and Sierra recreational vehicles because inaccurate gross vehicle weight rating labels could mislead owners about capacity.
ACCO Brands is recalling about 3.3 million Quartet magnetic and dry erase boards because sharp metal edges on the back can cause lacerations when removing the boards.
Heartland is recalling various trailer models because tire certification labels may contain inaccurate sizing or inflation information, potentially leading to tire failure.
Western / Scott Fetzer Company is recalling OxyTOTE Portable Oxygen System regulators due to a risk of ignition and rupture of the oxygen cylinder.
American Medical Systems is recalling 16,710 Sureflex 910 Lithotripsy Fibers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
American Medical Systems is recalling 16,710 Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Philips is recalling 13 GEMINI TF 16 Slice CT/PET systems worldwide due to four software defects in the Tumor LOC application that may affect treatment accuracy.
Philips is recalling 22 GEMINI TF 64 Slice CT/PET systems due to software defects that may cause incorrect tissue irradiation.
Philips is recalling two Gemini LXL CT/PET systems due to software defects that may cause incorrect radiation delivery to patients.
The FDA is recalling 5,786 sterile Double Basin Kits because the included Devon Light Gloves contain splits or holes that compromise sterility.
DePuy Orthopaedics is recalling ATTUNE FB PS Articulation Surface instruments because a small wire spring coil (Balseal) may detach and be left in the patient during surgery.
Philips is recalling two GEMINI TF Base CT/PET systems because four software defects in the Tumor LOC application may cause incorrect tissue irradiation.