State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2015 Lincoln MKC vehicles because the push-to-start button may be pressed accidentally, causing the engine to shut off and increasing crash risk.
Piaggio is recalling 2014-2015 Aprilia Shiver 750 and 2015 Caponord 1200 motorcycles because a defective output gear shaft may cause the rear wheel to lock up, increasing crash risk.
Ford is recalling certain 2014-2015 vehicles because a defective fuel pump may cause the engine to stall without warning, increasing the risk of a crash.
CoScentrix is expanding its recall of DD brand candles sold at Hobby Lobby because the high flame can ignite the wax surface, posing a fire hazard.
Pro Performance Sports is recalling SKLZ Recoil 360 Resistance Trainers because a weld can break, causing the cord to retract and injure users or partners.
Lance is recalling 2015 Slide-In Campers and Travel Trailers because awning mounting brackets may crack, causing the awning to fall and potentially injure people.
Star Ride Kids is recalling about 7,000 girls' pajama sets because they fail federal flammability standards, posing a burn risk.
Thor Motor Coach is recalling 154 model year 2015 motorhomes because defective awning screws could cause the awning to fall and injure people.
Safeway Inc is recalling Safeway Select French Salted Caramel Premium Ice Cream because peanut butter was used in the recipe but not listed on the label.
One and Zen is recalling Ginseng Kianpi Pill capsules because FDA analysis found undeclared dexamethasone and cyproheptadine, making the product an unapproved drug.
Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Hansen Medical is recalling Sensei X Robotic Catheter Systems because a mechanical clamp may become loose, causing the device to fall and potentially injure patients or users.
Nijiya Market is recalling approximately 359 pounds of frozen boneless beef products produced in Japan that were not presented for USDA inspection at the U.S. point of entry.
Polaris is recalling certain Victory motorcycles because a manufacturing defect may cause the fuel pump to seize, leading to stalling and an increased risk of a crash.
Roche is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Smiths Medical ASD, Inc. is recalling 10,000 units of Needle Pro Edge Safety Hypodermic Needles because the needle may not be captured in the safety sheath.
Roche Diagnostics is recalling 13,041 boxes of ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Roche is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Roche Diabetes Care is recalling ACCU-CHEK Tender I infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Perouse Medical is recalling Bard Caliber inflation devices that may fail to reach required pressure, potentially delaying angioplasty procedures.