State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kia is recalling 2016 Optima vehicles because the driver's frontal air bag may not deploy fully in a crash, increasing injury risk.
Hyundai is recalling specific 2015-2017 Sonata, Sonata Hybrid, and Elantra vehicles because the driver's frontal air bag may fail to fully deploy in a crash.
Terex is recalling 2001-2003 XT52, XT55, and XT60 aerial devices because lower booms may be made of insufficiently strong material, posing a risk of cracking and injury.
SouvNear is recalling about 650 women's silk scarves because they do not meet federal flammability standards, posing a burn risk.
Strick Trailers is recalling 2005-2009 single axle van trailers because rear impact guard gussets may increase injury risk in crashes.
Jayco is recalling 322 model year 2016 Octane Super Lite travel trailers because they may lack a 30-amp circuit breaker, increasing the risk of fire during an electrical short.
Dexcom Inc is recalling 18,004 G4 Platinum Pediatric Receivers because they may fail to provide intended audible alarms or alerts.
Dexcom Inc is recalling 41,925 G5 Mobile Receivers because they may fail to provide intended audible alarms or alerts to users.
Dexcom Inc is recalling G4 PLATINUM Receivers with Share because they may fail to provide intended audible alarms or alerts.
Dexcom Inc is recalling G4 PLATINUM Receivers because they may fail to provide intended audible alarms or alerts to users.
Figi's is recalling 8-ounce packages of Classic Marzipan because the product contains almonds that are not properly labeled on the ingredients list.
Dexcom Inc is recalling G4 PLATINUM receivers because they may fail to provide intended audible alarms or alerts for diabetes patients.
Dexcom Inc is recalling 19,586 G4 Platinum Pediatric Receivers because they may fail to provide intended audible alarms or alerts.
Forest River is recalling 2016 StarTrans Senator II transit buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.
Forest River is recalling 2015-2016 Starcraft Prodigy and Quest school buses because seats may separate from the base frame due to bolt failure.
Tri-Union Seafoods is recalling Chicken of the Sea canned tuna due to an equipment malfunction that may have caused the product to be undercooked.
Morrison's Pancake Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.
Gulf States Toyota is recalling 2015-2016 Toyota 4Runners with dealer-installed accessories because the load carrying capacity label may be incorrect, potentially leading to vehicle overload.
Arthrex is recalling 117 Deltoid Ligament Reconstruction Implant Systems because a component may not be sterile.
Bridgestone is recalling specific Firestone and Champion tires manufactured in March and April 2016 due to inconsistent rubber coverage that may cause tread separation.
Synthes (USA) Products LLC is recalling 289 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if a surgeon attempts to remove it.
GE Healthcare is recalling Aisys Carestation anesthesia devices due to a potential safety issue involving a momentary, self-correcting anesthetic agent bolus when using 21% oxygen.
GE Healthcare is recalling Aisys CS2 and upgraded Aisys anesthesia devices due to a potential safety issue involving a momentary, self-correcting anesthetic agent bolus when using 21% oxygen.
Synthes (USA) Products LLC is recalling 212 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.
ICU Medical is recalling 47 Diana Automated Compounding Systems because they may not meet accuracy specifications when mixing volumes under 5ml.