State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Linora Corporation is recalling WiFiRanger DC Step-Up power converters because they may overheat, increasing the risk of a fire.
Entrans is recalling 2017-2020 Heil AJB9-1040 Hybrid trailers because frame cracks may develop, affecting handling and increasing crash risk.
Newell Coach Corp. is recalling 2017-2020 P50 motorcoaches because a short wiper arm linkage may cause the wiper to rotate downward, reducing visibility and increasing crash risk.
Suzuki is recalling 2018-2019 Burgman 200 scooters because a transmission part may break, causing loss of power and increasing crash risk.
Micro Bird is recalling 2018-2019 G5 and T-Series school buses because a heavy-duty solenoid may overheat nearby components, potentially causing vehicle stoppage or fire.
Meijer is recalling Grand Gourmet french fry cutters because the blade can detach, posing a laceration hazard. No injuries have been reported.
Honda is recalling 19,138 vehicles because the front passenger air bag inflator may be installed incorrectly, potentially preventing proper deployment in a crash.
Alvogen is recalling Fentanyl Transdermal Systems because a customer reported a carton labeled 12 mcg/h contained 50 mcg/h patches.
Zydus Pharmaceuticals is recalling Acyclovir 400 mg tablets because one bottle was found to contain Carvedilol 6.25 mg tablets due to a label mix-up.
Mojave Foods is recalling El Guapo Chile Habanero pouches because they contain an unlabeled peanut allergen.
Navistar is recalling 2017 IC CE transit buses because the driver-side rear brakes may drag, posing a fire and injury risk.
Mojave Foods is recalling El Guapo Chile Pods due to an unlabeled peanut allergen. Consumers should check their pantry for the affected sizes and UPC codes.
Abbott is recalling ARCHITECT cSystems ICT Modules due to a potential for falsely elevated serum or plasma chloride results.
Navistar is recalling 2016-2020 IC Bus school buses because the driver-side rear brakes may drag, potentially causing fire or injury.
Par Pharmaceutical is recalling Mycophenolate Mofetil for Injection due to the presence of particulate matter and a glass fragment in one vial.
Zydus Pharmaceuticals is recalling Carvedilol 6.25 mg tablets because one bottle was found labeled as Acyclovir 400 mg.
Sagent Pharmaceuticals is recalling 75,825 vials of Ketorolac Tromethamine Injection because microbial growth was detected during a routine manufacturing simulation.
Alpha Omega Engineering is recalling 29 Neuro Omega Systems because improperly connected cables may cause high charge density, leading to tissue harm.
Conmed Corporation is recalling specific lots of the Anchor Tissue Retrieval System because seal defects may compromise the product's sterility.
Siemens is recalling two Cios Alpha mobile X-ray systems because continuous high-output operation may cause premature failure of radiation components.
Hush is recalling anesthetic gels, sprays, and foam soaps because the packaging does not meet child-resistant closure requirements, posing a risk of poisoning to young children.
Zimmer Biomet is recalling 5,885 T7 Driver Cannulated AO units because they may fracture, bend, or shear during use.
Conmed Corporation is recalling Anchor Tissue Retrieval Systems due to seal defects that may compromise sterility. The recall affects 7,930 units distributed in the US and 13 other countries.
ConMed is recalling Anchor Tissue Retrieval Systems because voids or partial seals may compromise sterility. The recall covers units distributed worldwide.
ConMed is recalling Anchor Tissue Retrieval Systems due to seal defects that may compromise sterility. The recall covers 5,034 units distributed worldwide.