State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arrow International is recalling 18,124 Pressure Injectable Multi-Lumen CVC Kits because they lack required clinical safety checklists.
Arrow International is recalling 18,124 percutaneous sheath introducer kits because they lack required central line insertion checklists and procedure notes.
Arrow International is recalling 18,124 central venous catheterization kits because they are missing the Central Venous Catheter Placement Procedures Note and Central Line Insertion Checklist.
Arrow International is recalling 18,124 central venous catheter kits nationwide because they lack required procedural notes and insertion checklists.
Ethicon is recalling specific lots of the DERMABOND PRINEO Skin Closure System because the adhesive may not dry within the specified time and may fall off.
CooperSurgical is recalling 13 units of 2 MHz Waterproof OB probes because they were incorrectly labeled as 3 MHz probes.
Arrow International is recalling 18,124 percutaneous sheath introducer kits because they are missing the Central Venous Catheter Placement Procedures Note and Central Line Insertion Checklist.
Arrow International is recalling 18,124 central venous catheter kits nationwide because they lack required clinical safety checklists.
Akorn, Inc. is recalling 4,128 bottles of Triamcinolone Acetonide Lotion, USP 0.1% due to high impurity levels. The product was distributed nationwide and in Puerto Rico.
Newmar is recalling 2011-2017 Mountain Aire, Dutch Star, and Ventana motorhomes because the power steering hose may rub against the starter motor, causing fluid leaks or electrical arcing.
Polaris is recalling 2015-2018 Slingshot motorcycles because improperly welded seat brackets may fail, increasing crash injury risk.
Daimler Trucks North America is recalling 2017-2019 Western Star trucks because a power stud may contact the bulkhead, causing an electrical arc that increases fire risk.
Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses school buses because a wall mounting bracket may crack, causing seats to detach in a crash.
Daimler Trucks North America is recalling 2014-2019 Thomas Built Buses Saf-T-Liner C2 school buses with propane engines due to a fuel line chafing risk that could cause a leak and fire.
Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses transit models because a wall mounting bracket may crack, increasing injury risk in a crash.
Winnebago is recalling 2018-2019 Intent motorhomes because exterior rearview mirrors may fall off while driving, increasing crash risk.
Daimler Trucks North America is recalling 2018-2019 Freightliner Custom Chassis XCS motorhome chassis because a valve stem stabilizer may dislodge, potentially causing tire damage and increasing crash risk.
Ferrari is recalling 2009-2011 California and 2010-2011 458 Italia vehicles because passenger air bag inflators may explode during a crash, posing a risk of serious injury or death.
Lazy Daze is recalling 2012-2017 motorhomes because certain fire extinguishers may clog or detach, potentially failing to work during a fire.
Keystone RV Company is recalling 2018 Passport recreational trailers because the spare tire carrier may detach, increasing crash risk.
SpeeCo and Woods are recalling 4-way wedge accessories for hydraulic log splitters because they can detach and strike users, causing injury.
Columbia Northwest is recalling 2013-2018 Somerset E3 trailers because certification labels may lack Gross Axle Weight Rating information, potentially leading to overloading.
Pfizer is recalling 53,600 vials of Hydromorphone Hydrochloride Injection due to confirmed customer complaints of empty or cracked glass vials.
Blue Moose of Boulder, LLC is recalling 504 units of All-Natural Ciolo Nut-Free Basil Pesto because the product contains undeclared tree nuts.
Alden Optical is recalling 23 units of HP49 Sphere Daily Wear Soft contact lenses because they lack sterility assurance.