State
73,806 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Honda is recalling 2018 Accord and 2019 Insight vehicles because the backup camera display may not function properly, increasing crash risk.
Jaguar Land Rover is recalling 2018 Discovery, Range Rover, and Range Rover Sport vehicles because the Automatic Emergency Braking system may disable without warning, increasing crash risk.
Altec Industries is recalling 2018 cranes, digger derricks, and aerial devices because overtightened fasteners may break, potentially causing the platform to separate from the vehicle.
AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
New Flyer is recalling 386 XDE40, XDE60, and XDE35 transit buses because pressure switches may fail, causing a loss of drive and increasing crash risk.
AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
GE Medical Systems is recalling Vivid E7 ultrasound systems because the power cord may break and expose electrical conductors, creating a risk of electric shock.
AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
BMW is recalling 2018-2019 X6 and X6 M vehicles because wheel bolts may not have been properly tightened, which could loosen and break, increasing crash risk.
AvKARE is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Highland Ridge RV is recalling 2019 Open Range and Mesa Ridge travel trailers because missing inner bearing races may cause hub failure and increase crash risk.
McKesson is recalling 1,531 cartons of Megestrol Acetate Oral Suspension because the drug is supra-potent. The recall is voluntary and nationwide.
Jayco is recalling 2019 White Hawk, Jay Flight, and Jay Flight SLX travel trailers because missing inner bearing races may cause hub overheating and axle separation.
McKesson Israel Ltd. is recalling McKesson Cardiology Hemo software version 13.0 because the Real Time Monitor may fail to display physiological signals under certain circumstances.
Steris Corporation is recalling 2,889 V-PRO low temperature sterilization systems because they may fail to detect expired sterilant cups after a power cycle.
GE Medical Systems is recalling 12,426 Vivid 7 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.
GE Medical Systems is recalling 12,426 Vivid E95 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.
GE Medical Systems is recalling Vivid E90 ultrasound systems because the power cord may break and expose electrical conductors, posing a risk of shock.
GE Medical Systems is recalling 12,426 LOGIQ 9 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.
Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because a blocked refrigerator roof vent may increase fire risk or allow carbon monoxide entry.
GE Medical Systems is recalling Vivid E80, E90, and E95 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.
GE Medical Systems is recalling 12,426 LOGIQ E9 ultrasound systems because the power cord side may break, exposing electrical conductors and creating a risk of electric shock.
GE Medical Systems is recalling 12,426 Vivid E9 ultrasound systems because the power cord may break and expose electrical conductors, posing a risk of electric shock.
Quasar Bio-Tech is recalling 6,783 Pure Rayz Light Therapy Systems because the packaging and manuals make claims about collagen and elastin production that were not cleared by the FDA.