State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Gulf Stream is recalling 2016-2018 Conquest and B Touring Cruiser motorhomes because they lack required intermediate side marker lights, increasing crash risk.
Ducati is recalling 2018 Panigale V4 motorcycles because fuel may leak from the gas tank valve plug, increasing the risk of fire.
Ducati is recalling 2018 Panigale V4 motorcycles because fuel may spray out of the tank when the cap is opened, increasing fire risk.
Nissan is recalling 2016-2018 Titan and Titan XD trucks because missing labels may allow owners to overload the vehicles, increasing crash risk.
Forest River is recalling 2017-2019 Crossfit coaches because incorrect weight placards may lead to vehicle overloading and increased crash risk.
Group Rossignol is recalling LOOK Pivot ski bindings because the heel piece can loosen, posing a fall hazard to skiers.
Newmar is recalling 2018 motorhomes because loose electrical connections in the breaker box may overheat and increase the risk of a fire.
KME is recalling 38 Predator fire trucks because improperly routed hydraulic hoses may contact electrical components, creating a fire risk.
Isuzu is recalling 2018-2019 NPR models because a brake switch retainer may not be secured, potentially disabling acceleration and increasing crash risk.
Chrysler is recalling 2018 Jeep Wrangler vehicles because the rear underbody ladder rail may corrode, potentially weakening the floor pan and loosening the rear seat mount.
Forest River is recalling 2018-2019 FR3 and Georgetown recreational vehicles because the entry door latch may not engage fully, allowing the door to open unexpectedly while moving.
General Motors is recalling 2018 Buick Regal vehicles because rear seat belts may be improperly routed, potentially failing to restrain passengers in a crash.
Forest River is recalling 2018 Salem recreational trailers because the federal placards list incorrect tire pressure, which may lead to under-inflation and increased crash risk.
L.L.Bean is recalling Allagash fixed blade hunting knives because the blade can cut through the leather sheath, posing a laceration hazard.
Natural Grocers by Vitamin Cottage is recalling Organic Coconut Smiles because the product tested positive for Salmonella.
Volkswagen Group of America is recalling specific Audi models because a coolant pump defect may cause overheating or short-circuiting, increasing the risk of a fire.
Conagra Brands is recalling approximately 135,159 pounds of Salisbury steak products due to possible bone contamination. The recall follows reports of minor oral injuries.
GE Healthcare is recalling 1,742 units of the Monica Novii Wireless Patch System because incorrectly reconnected cables may cause fetal and maternal heart rate signals to be displayed swapped.
Baxter Healthcare is recalling 3,440 Prismaflex Control Units worldwide due to reports of operators failing to follow safe unloading instructions and software errors in specific versions.
C.R. Bard is recalling specific lots of HydroSil Gripper Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
C.R. Bard is recalling Magic 3 Intermittent Catheters because some units were caught in the sterile barrier seal or cut.
GE Healthcare is recalling 355 Monica IF24 Interface Systems because incorrectly reconnected cables can cause fetal and maternal heart rate signals to be displayed incorrectly.
C.R. Bard is recalling Personal Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
Arrow International is recalling 930 Radial Artery Catheterization Kits because the included povidone iodine prep pads are labeled with an incorrect 36-month shelf life instead of 24 months.
GE Healthcare is recalling 569 units of Centricity PACS-IW because a database error may cause image series to be missing from exams without user notification.