State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Micro Bird is recalling 2014-2016 G5 and MB II transit buses because a wheel bolt may be insufficiently torqued, posing a risk of vehicle misalignment and loss of control.
Temsa is recalling 2008-2016 TS35C buses because a steering gearbox bracket fastener may loosen, potentially causing loss of vehicle control.
Macy's is recalling Martha Stewart Collection 10-piece cookware sets because metal discs on the frying pans can pop off and injure users.
Chrysler is recalling 2011-2013 Dodge Durango and Jeep Grand Cherokee vehicles because sun visor wiring may short circuit, increasing the risk of a vehicle fire.
Ferrari is recalling 119 model year 2016 488 GTB vehicles because a fuel line connection may leak vapor, increasing fire risk.
BMW is recalling 2015 i8 vehicles because improperly drilled holes in the stability control unit may impair braking and handling, increasing crash risk.
Tiffin is recalling 2007-2015 motorhomes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.
A. L. Schutzman Company, Inc. is recalling Ashdon Farms Honey Mustard Mix because the packaging lists whey but fails to declare milk in the 'Contains' statement.
Zenobia Co. is recalling My Spice Sage Ground Flax Seed Meal due to the possible presence of Salmonella. The product was sold nationwide via the internet.
Hyundai is recalling 2011-2012 Elantra vehicles because an electronic stability control sensor malfunction may cause unexpected braking and reduced engine power, increasing crash risk.
Remel Inc is recalling specific lots of Gentamicin Antimicrobial Susceptibility Testing Discs because the antibiotic concentration may be insufficient, potentially leading to incorrect test results.
Chrysler is recalling 2015 Jeep Compass and Patriot vehicles because a power steering hose clamp may be installed incorrectly, increasing the risk of a fire.
Insulet Corporation is recalling 5,179 boxes of OmniPod Insulin Management Systems because the needle mechanism may fail to deploy or deploy with a delay.
Bruce Foods Corporation is voluntarily recalling 816 cases of Del Pasado Dice Green Chiles because the product may contain metal.
A. L. Schutzman Company, Inc. is recalling Girl Scouts Honey Mustard Pretzel Mix because the product lists whey but fails to declare milk in the 'Contains' statement.
Insulet Corporation is recalling OmniPod Insulin Management Systems because the needle mechanism may fail to deploy or deploy with a delay.
GE Medical Systems is recalling 45 Optima IGS 320 systems due to a potential safety issue involving non-recoverable loss of displayed imaging.
Navistar is recalling certain 2007-2015 IC Bus transit models because wheelchair lift bearings may move out of position, causing the platform to fall.
H&H Trailers is recalling 1,847 model year 2015-2016 trailers because aluminum gate hinges may bend or break, potentially causing the gate to open unexpectedly.
Stryker is recalling 120 units of Guidewire Introducer Needles shipped after expiration or with minimal time remaining due to infection risk.
Verathon is recalling GlideScope Video Laryngoscope blades because silicone adhesive may fail, causing the blade halves to separate during use.
Honda is recalling specific VT750 motorcycles because a wiring defect may cause the engine to stall while riding, increasing crash risk.
bioMerieux, Inc. is recalling MYLA Clinic Patch 3.2.0 CD software because it may link test results to incorrect patient records when connected to specific laboratory systems.
bioMerieux is recalling MYLA Clinic Patch 3.3.0 software because it may link test results to incorrect patient records when connected to specific laboratory systems.
bioMerieux is recalling MYLA CLI software versions 3.x to 4.1 because it may link test results to incorrect patient records.