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.
Daimler Trucks North America is recalling 2013-2015 Freightliner Cascadia CNG vehicles because hot exhaust near the pressure relief device may cause gas release and fire.
Honda is recalling 2010, 2012, and 2013 VFR1200F motorcycles because driveshaft universal joint bearings may wear prematurely, potentially causing the joint to separate or break.
Tiny Idahomes is recalling 2014-2016 RVs equipped with specific Atwood water heaters that may overheat water, posing a scalding risk.
Triple E RV is recalling 2014 Regency GT motorhomes because a water heater valve may cause water to overheat, potentially releasing steam and scalding the operator.
Mitsubishi is recalling 2014-2015 Mirage vehicles because water and salt corrosion may delay frontal air bag deployment in a crash.
Cost Plus World Market is recalling about 2,700 reading chairs because the front legs can bend or break, posing a fall hazard.
ShowHauler Trucks is recalling one 2013 ShowHauler motorhome because a defective water heater valve may cause water to overheat, posing a scalding risk.
TN Juice Bar is recalling 137 units of the Refine 3-Day Cleanse juice kit nationwide due to unpasteurized juice with elevated pH levels and unlabeled almond milk.
Ford is recalling 2013 Explorer, Taurus, Flex, Lincoln MKS, and MKT vehicles because a cracked fuel delivery module may leak fuel and cause a fire.
North Central Industries is recalling about 2,600 Great Grizzly brand fireworks fountains because the rear plug can dislodge while lit, causing burn injuries.
NxStage Medical is recalling 16 System One S Cycler units due to a software error causing inaccurate fluid removal.
Covidien LLC is recalling 365 units of Palindrome Precision Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.
Qualgen is recalling 4,221 vials of compounded Estradiol USP pellets nationwide because deficient practices may have impacted sterility assurance.
Philips is recalling HeartStart MRx Monitor/Defibrillators because a software issue may cause the automated Ready-For-Use test to stop in an abnormal state when the device is turned off.
NxStage Medical is recalling 323 System One S Cycler units due to a software error that may cause inaccurate fluid removal during hemodialysis.
Qualgen is recalling 10,885 vials of compounded Testosterone USP pellets nationwide due to deficient practices that may impact sterility assurance.
Covidien LLC is recalling 10 units of Palindrome Precision Chronic Catheter Kits due to incorrect packaging with a 90-degree bend at the distal tip.
Masimo is recalling Rainbow Reusable Sensors because incompatible configurations may cause no readings or inaccurate SpCO and SpMet results.
Felt Bicycles is recalling 645 model year 2015 mountain bikes because the carbon fiber seatposts can crack and break, posing injury and fall hazards.
Siemens Healthcare Diagnostics is recalling 3,601 Dimension Vista magnesium reagent cartridges due to erroneous low results that may affect patient and quality control testing.
Ford is recalling specific 2013 Escape and 2013-2014 Focus ST vehicles because engine wiring splices may send incorrect signals, causing hesitation or stalling.
Covidien LLC is recalling 150 units of Palindrome Precision Chronic Catheter Kits due to incorrect packaging with a 90-degree bend at the distal tip.
Covidien LLC is recalling 280 units of Palindrome Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.
Covidien LLC is recalling 160 units of Palindrome Precision Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.
Leica Microsystems is recalling specific lots of Novocastra CD10 antibody reagents because they are not stable up to the labeled expiry date.