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.
The Children's Place is recalling boys' varsity jackets because metal snaps could detach and pose a choking hazard to young children.
Turtle Top is recalling certain 2012 Van Terra XL and Odyssey XL transit buses because their windows may not meet federal safety loading requirements.
Forest River is recalling 634 model year 2015-2016 XLR trailers because strained wiring at the external power inlet may loosen and arc, increasing the risk of a vehicle fire.
Draeger Medical is recalling 373 Fabius MRI anesthesia machines because their parts can be loosened by the magnetic field of MRI equipment.
Forest River is recalling 2015 Palomino PaloMini vehicles because axle tube cambers may be installed upside down, increasing crash risk.
Philips is recalling 159 Ingenuity CT scanners due to software errors affecting dose control, image artifacts, and heart rate measurement.
Otto Bock Healthcare GmbH is voluntarily recalling 3R62 Pheon prosthetic knee joints because the locking function may fail, potentially causing a fall.
Felling Trailers is recalling 92 model year 2016 FT-6T tilting trailers because improper fender placement may cause tires to rub, potentially leading to tire failure and a crash.
DRV Suites is recalling specific fifth wheel travel trailers because front side reflex reflectors are located above the maximum height of 60 inches, failing to comply with FMVSS 108.
Hamilton Medical is recalling 248 Hamilton-G5 ventilators because the display can freeze, preventing users from operating the device while ventilation continues.
The FDA is recalling OxiMax N-560 Pulse Oximeters because missing display segments may cause users to misinterpret oxygen saturation and pulse rate data.
FDA is recalling OxiMax N-65 handheld pulse oximeters because missing display segments may cause users to misinterpret oxygen saturation and pulse rate data.
Disney Store is recalling about 300 Gadget Pencil Cases because the magnets on the lids can detach and be swallowed, posing a serious internal injury risk to children.
Prism Medical is recalling 409 P-600 Portable Ceiling Lifts because sling loops may not stay attached to the carry bar hooks.
Prism Medical is recalling P-440 Portable Ceiling Lifts because sling loops may not stay attached to the carry bar hooks.
MZB is recalling about 1.9 million children's watches because the case-back can detach, exposing the interior to water and causing skin irritation or chemical burns.
Dairy Farmers of America is recalling specific fat-free Swiss cheese products because plastic film strips may remain attached to the slices.
Siemens is recalling ACUSON S 1000, S 2000, and S 3000 ultrasound systems due to a potential measurement error in the Doppler manual trace tool that could lead to misdiagnosis.
Philips is recalling 82 Ingenuity Core CT systems due to software errors affecting image quality, dose control, and heart rate monitoring.
Philips Medical Systems is recalling two Brilliance iCT SP CT systems due to software issues affecting image quality, dose control, and heart rate measurement.
Philips is recalling 38 Brilliance iCT CT systems due to software errors affecting dose control, heart rate measurement, and image artifacts.
Newmar is recalling 82 model year 2015-2016 Mountain Aire, King Aire, and Essex motor homes because the air suspension control module may lose power, potentially affecting vehicle control.
Philips is recalling 139 Ingenuity Core 128 CT scanners due to software errors affecting image quality, dose control, and heart rate monitoring.
Winnebago is recalling 2012-2016 Era recreational vehicles because certification labels list incorrect front tire inflation pressures, which could lead to tire failure.
Dairy Farmers of America is recalling specific Sandwich Mate cheese slices because a piece of plastic film might remain attached to the product.