State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Audi is recalling one 2020 Q3 because the driver's seat frame may be incorrectly bolted to the seat rail, increasing injury risk in a crash.
Continental Automotive Systems is recalling Vitesco NG2 Fuel Delivery Modules where a plastic burr may block the mixing tube, causing insufficient fuel supply and vehicle stalling.
Shyft Group is recalling 2021 Utilimaster Aeromaster vehicles because a body mount bracket may chafe brake lines, potentially reducing braking ability and increasing crash risk.
Daimler Trucks North America is recalling 2018-2019 Freightliner and Western Star trucks because a clutch component may fail, allowing the vehicle to move unexpectedly.
Akron Brass is recalling Weldon V-Mux Vista IV LCD displays used in emergency vehicles because they may lock up due to voltage spikes, potentially delaying emergency efforts.
Zero Motorcycles is recalling 2021 SR, S, DSR, DS, FX, and FXS models because the DC-DC converter may shut off, disabling ABS and lights.
General Motors is recalling 2,781 2020 Buick, Cadillac, Chevrolet, and GMC SUVs because a fuel pump defect may cause the engine to stall without warning.
Prime-Time Specialty Vehicles is recalling 2014-2019 Ram ProMaster Paratransit vehicles because the transmission shifter cable may disconnect, causing unintended movement.
General Motors is recalling 1,788 vehicles because a previous repair may have been improper, causing the driver's seat belt tensioner cable to fatigue and separate.
Ford is recalling certain 2019-2020 Transit Connect vehicles with 2.5L engines because faulty PCM software can cause engine overheating and increase fire risk.
Ford is recalling 2020 Escape vehicles because the Body Control Module may fail to detect low tire pressure, increasing crash risk.
Peloton is recalling PR70P clip-in pedals fitted on bikes sold between July 2013 and May 2016 because they can break unexpectedly, causing laceration injuries.
Genie is recalling 2020 TZ-34 and TZ-50 trailer-mounted boom lifts because under-tightened bolts may affect stability and increase injury risk.
Sales BSD is recalling Homerygardens extension cord splitters because the wire size cannot handle the appropriate amp load, posing a fire hazard.
Biomet is recalling OnPoint Scope Procedure Kits because they were not properly aligned with the gamma sterilization group, resulting in improper sterilization.
Roche Diagnostics is recalling BenchMark ULTRA Advanced Staining Systems due to a risk of fluid leaks causing electrical shorts, heat, and fire.
Daimler Vans USA is recalling 2020 Mercedes-Benz Sprinter vans because damaged brake hoses may leak fluid, increasing crash risk.
Roche Diagnostics is recalling the DISCOVERY ULTRA Advanced Staining System due to fluid leaks that can cause electrical shorts, heat, and smoke.
Bombardier is recalling 2020 Can-Am Ryker motorcycles because improperly installed front wheels may separate, increasing crash risk.
AB ULAX is recalling 1500 Flex Heat and Moisture Exchangers because they may disconnect from the respiratory circuit, potentially causing hypoxia or death.
Biomet is recalling Regenerex Primary Taper Caps because they were not properly aligned for gamma sterilization, potentially leaving them unsterilized.
Toyota is recalling 2020 Highlander and Highlander Hybrid vehicles because incorrect seat trim covers may prevent side airbags from deploying properly, increasing injury risk in a crash.
Encore Medical is recalling 190 units of DJO EMPOWR Tibial Knee Punch Handles because the retaining pin may fall out, potentially leaving debris in the joint space.
Medline Industries is recalling 16 non-sterile Left Heart Kits sold to facilities without sterilization capabilities. The kits were intended to be sterilized prior to use.
Biomet is recalling ARTHROSIMPLICITY KIT EU units because they were not properly aligned with the gamma sterilization group, resulting in improper sterilization.