State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arthrex, Inc. is recalling 47 units of the Fibulock Fibular Nail Instrument Set due to a potential for blockage of the Hub Attachment Tube.
Pharmaceutical Associates Inc. is recalling Nystatin Oral Suspension because it failed potency testing at 12 months. Patients should stop using the product and consult their healthcare provider.
GE Healthcare is recalling 62 SIGNA Pioneer MRI systems because an installation issue may cause incorrect dates on medical images.
Cummins is recalling PowerDrive EV drivetrains for school buses, step vans, and medium-duty trucks because a connector may unplug, causing sudden loss of drive power and power steering.
Hyundai is recalling specific Elantra, Elantra Touring, Santa Fe, and Entourage models because moisture in the ABS module can cause an electrical short and engine compartment fire.
Goodyear is recalling specific Fortera HL tires because a manufacturing issue may cause belt separation, increasing the risk of a crash.
KZRV is recalling 2020 Connect SE trailers because propane lines may be routed too close to tires, creating a fire risk if damaged by road debris.
McElrath Trailers is recalling 2016-2020 VX30-800 and VX50-800 trailers because structural frame welds may crack, increasing crash risk.
Volkswagen Group of America is recalling specific Audi A8, A4, TT, and A6 models because driver air bag inflators may absorb moisture, potentially causing improper deployment in a crash.
Triple E is recalling 237 2020 Unity, Wonder, and Serenity motorhomes because twisted or kinked propane lines may leak and cause a fire.
Volkswagen is recalling 2018 Atlas vehicles because an incorrectly manufactured air bag sensor may delay or disable deployment, increasing injury risk in crashes.
Vac-Tron is recalling 2016-2020 LPSDT trailers because missing exterior lighting and reflective markings may reduce visibility and increase crash risk.
Jaguar Land Rover is recalling 2020 Discovery vehicles because second-row seat frames may lack fasteners, potentially failing to secure occupants in a crash.
General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because a software error may disable electronic brake assist, increasing crash risk.
K-Apparel is recalling about 2,200 TINFL children's lounge pants because they fail federal flammability standards, posing a burn risk to children.
Polaris is recalling about 760 Model Year 2019 Pro XD utility vehicles because the rear brake line can puncture, causing rear brake failure and posing a crash hazard.
Bobcat is recalling 2017-2018 3650 utility vehicles because a punctured rear brake line can cause brake failure, posing a collision hazard.
BMW is recalling 2020 X7 xDrive40i and xDrive50i vehicles because rear reflex reflectors may not reflect enough light, increasing crash risk.
Pier 1 is recalling approximately 6,000 upholstered swivel desk chairs because the legs can break, posing fall and injury hazards.
Polaris is recalling 2017-2018 Brutus utility vehicles because a rear brake line can puncture, causing brake failure and a crash hazard.
Astrochef LLC is recalling Banquet pepperoni stuffed pizza sandwiches due to misbranding and undeclared soy, a known allergen.
GE Healthcare is recalling 3,319 Carestation anesthesia systems worldwide due to a potential loose cable connection that could cause loss of mechanical ventilation.
Polymer Technology Systems is recalling 44,448 CardioChek Plus Professional Analyzers because a battery terminal defect can cause reverse contact and potential overheating.
Entropic Labs is recalling SARM RAD-140 capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
GE Healthcare is recalling 280 Carestation anesthesia systems worldwide due to a potential loose cable connection that could cause a loss of mechanical ventilation.