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.
Hologic is recalling 337 I-View Contrast Enhanced Digital Mammography systems due to a calibration issue that prevents visualization of contrast uptake.
Tosoh Bioscience Inc is voluntarily recalling 1,085 units of ST AIA-PACK ACTH in vitro diagnostic reagents distributed nationwide in the US.
Tosoh Bioscience Inc is recalling AIA-PACK B12 reagents because fluorescein interference may cause inaccurately elevated Vitamin B12 test results.
Tosoh Bioscience is recalling 992 units of ST AIA-PACK Homocysteine reagents used for in vitro diagnostic testing. The voluntary recall covers all lots distributed nationwide.
Arcimoto is recalling 2018 FUV motorcycles because incorrect machining of the transmission case may cause premature gearbox failure, potentially immobilizing the vehicle and increasing crash risk.
Arcimoto is recalling 2017-2018 FUV motorcycles because the front suspension and steering system may loosen or wear, potentially causing a loss of steering control.
Arcimoto is recalling 2017 FUV motorcycles because the brake system design may fail to meet federal stopping distance requirements, increasing crash risk.
Arcimoto is recalling 2017 FUV motorcycles because incorrect fittings in the braking system may cause fluid leaks, reducing brake effectiveness and increasing crash risk.
Arcimoto is recalling 2017-2018 FUV motorcycles because the headlights may be spaced too far apart, making the vehicle difficult to recognize as a motorcycle in the dark.
Arcimoto is recalling 2017-2018 FUV motorcycles because the rear light assembly lacks required side reflex reflectors, reducing visibility and increasing crash risk.
Arcimoto is recalling 2017-2018 FUV motorcycles because they lack a service brake warning light. This defect increases the risk of a crash if the brake system malfunctions.
Arcimoto is recalling 2017-2018 FUV motorcycles because the seat may not support the driver in a crash, increasing injury risk.
Arcimoto is recalling 2017-2018 FUV motorcycles because front turn signals are not positioned as required by federal safety standards, potentially reducing visibility.
Subaru is recalling 2018 Legacy, Outback, and BRZ vehicles because a software issue may prevent the rearview camera from displaying an image while backing up.
Arcimoto is recalling 2017-2018 FUV motorcycles because increased battery resistance may cause the propulsion system to shut down unexpectedly, increasing crash risk.
R. L. Zeigler Co. is recalling Red Hot chicken and pork sausage products due to possible metal contamination. No illnesses have been reported.
Hyundai is recalling 2011-2014 Sonata and 2013-2014 Santa Fe Sport vehicles because a fuel pipe may leak, increasing the risk of a fire.
Arcimoto is recalling 2017-2018 FUV motorcycles because they lack required certification labels, which may prevent owners from verifying safety recall status.
Forest River is recalling 2019 Salem and Wildwood recreational trailers because the power cord hatch is located above the water heater exhaust, which may cause melting and increase fire risk.
Results RNA, LLC is recalling Lubrisine eye drops nationwide due to lack of sterility assurance and the presence of undeclared colloidal silver.
COVIDIEN LLC is recalling 9,593 Puritan Bennett 980 ventilators worldwide due to a software update affecting external USB drive performance and GUI functionality.
Tris Pharma is recalling specific lots of Infants' Ibuprofen because they may contain a higher concentration of the active ingredient.
FDA is recalling specific lots of the Covidien Emprint Short Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft during use, potentially remaining in the patient.
Tris Pharma is recalling 19,488 bottles of Infants' Ibuprofen due to potential higher-than-labeled ibuprofen concentrations.
Tris Pharma is recalling specific lots of infants' ibuprofen oral suspension because they may contain a higher concentration of the active ingredient.