State
73,741 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,821 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 1,485 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mercedes-Benz is recalling two 2018 vehicles because the steering coupling may not be locked, which could reduce steering ability and increase crash risk.
Micro Bird is recalling 2015-2018 CT-Series buses because foldaway seats may not stay locked during a crash, increasing injury risk.
Rosenbauer America is recalling 2017-2018 Fire Apparatus vehicles because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Altec is recalling 2017-2018 Aerial Devices, Service Bodies, and Digger Derricks because Whelen accessory brake lights may illuminate without the brake pedal being pressed.
Keystone RV Company is recalling 2018-2019 Raptor recreational trailers because an incorrectly routed propane line allows the grill to be stored while lit, increasing fire risk.
Kawasaki is recalling 1,173 2018 Z900 and Z900RS motorcycles because the rear brake hose or sensor wire may contact the tire, risking brake failure or ABS malfunction.
Kawasaki is recalling about 1,000 Mule Pro off-highway utility vehicles because the rollover protection structure may fail to protect occupants, posing an injury hazard.
Meijer is recalling about 25,000 Falls Creek Kids infant and toddler hoodies because the zipper slider can detach, posing a choking hazard to young children.
Skip Hop is recalling Tuo convertible high chairs because the legs can detach from the seat, posing fall and injury hazards to children.
General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 Crew Cab vehicles because the passenger-side air bag may not inflate properly in a crash.
Chukar Cherry Company is recalling 569 pouches of Ultra Dark Chocolate Cocoa Pecans because the product contains milk, which is not listed on the label.
NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.
Volkswagen is recalling 2018 Golf R vehicles because a fuel hose connector may detach, causing a leak that increases fire risk.
Eurotrol Inc. is recalling HemoTrol Level 2 hematology quality control mixtures because microbial contamination causes incorrect measurement results.
NxStage Medical is recalling 7,275 units of PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.
Synaptive Medical Inc is recalling 37 units of BrightMatter Guide software due to a defect that occurs when switching between specific port trajectories during surgery.
Chukar Cherry Company is recalling Ultra Dark Chocolate Amaretto Rainier Cherries because the product contains milk, which is not listed on the label.
Volkswagen is recalling 2015-2016 Audi A6 and 2015 A7 vehicles because an incorrectly inserted auxiliary heater connector may overheat and cause a fire.
Chukar Cherry Company is recalling Organic Ultra Dark Orange Chocolate Tart Cherries because the product contains milk, which is not listed on the label.
Chukar Cherry Company is recalling 502 pouches of Organic Ultra Dark Vanilla Chocolate Rainier Cherries because the product contains milk, which is not listed on the label.
Maquet Cardiovascular is recalling QUADROX-i Neonatal membrane oxygenators due to a potential for blood leakage at the blood inlet connector when using a specific reducing screw adapter.
NxStage Medical is recalling specific lots of PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.
NxStage Medical is recalling PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.
Chukar Cherry Company is recalling Ultra Dark Chocolate Black Forest Cherries due to the unintentional presence of milk, which is not listed on the label.
Maquet is recalling QUADROX-i Neonatal membrane oxygenators because a specific reducing screw adapter may cause blood leakage at the inlet connector.