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.
Mack Trucks is recalling 57 model year 2017 Pinnacle CHU and CXU trucks because improperly cured tires may cause partial tread separation, increasing crash risk.
Jayco is recalling 137 model year 2017 Seismic travel trailers because an incorrect fuse may fail to protect the circuit, increasing the risk of an electrical fire.
Newmar is recalling 2017 King Aire, Essex, London Aire, and Mountain Aire motorhomes because a power steering pump defect may cause intermittent loss of steering assist.
Aqua Lung is recalling about 53,000 Powerline inflators because the inflation button can remain depressed, causing uncontrolled ascent and posing injury and drowning hazards.
Subaru is recalling 2017 Legacy and Outback vehicles because the knee guard bracket may not be properly attached, increasing injury risk in crashes.
GITI Tire is recalling specific Primewell, GT Radial, and Dextero tires that may develop sidewall cracks, potentially leading to air loss and tire failure.
Wildhorn Outfitters is recalling about 9,700 Outpost camping hammocks and suspension kits because cinch buckles can fail, posing a fall hazard.
Gleason is recalling about 120,000 Milwaukee hand trucks because plastic wheel rims can break, posing a laceration hazard.
The Anspach Effort, Inc. is recalling Light Adaptors for Small Battery Drive and Small Battery Drive II devices due to a potential risk of bursting from excessive internal pressure.
Bounce Life Style HQ is recalling Cashew Cinnamon products due to potential Listeria monocytogenes contamination from recalled sunflower kernels.
Bounce Life Style HQ is recalling Bounce Energy Ball Cashew & Pecan Vitality Lift due to potential Listeria monocytogenes contamination from recalled sunflower kernels.
Continental is recalling specific Crosscontact LX20 tires due to insufficient adhesion that can cause tread loss and increase crash risk.
Bounce Life Style HQ is recalling Apple Cinnamon Protein Energy Balls due to potential Listeria monocytogenes contamination from sunflower kernels.
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels.
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels, potentially affecting patient safety.
The Anspach Effort, Inc. is recalling 1,833 Small Battery Drive adaptors worldwide because they may generate excessive internal pressure and burst.
Daimler Trucks North America is recalling 162 model year 2017 Thomas Built Buses Saf-T-Liner C2 school bus chassis because the brake transmission shift interlock may be inoperable.
Universal Trailer Cargo Group is recalling 89 aluminum snowmobile trailers because cross winds may cause them to tip or lift, potentially tearing the couplers.
Zyno Medical LLC is recalling 47,989 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients.
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels. The recall affects strips and kits distributed in the US and internationally.
Spacelabs Healthcare is recalling Xhibit Telemetry Receivers because the system may go offline or lock up, potentially failing to display alarms.
Siemens Medical Solutions is recalling 103 PRIMUS linear accelerators to install a software patch addressing several safety issues.
Zyno Medical LLC is recalling 78,063 sterile administration sets due to a potential filter leaking defect. The sets are distributed nationwide for use with infusion pumps or gravity feed.
Spiegelberg is recalling 22 Brain Pressure Monitoring System probes due to air chamber shrinkage that caused false high readings in the lower measuring range.
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels.