State
73,741 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,821 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 1,485 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Epic Pharma is recalling Estradiol 2 mg tablets because a foreign tablet was found in a dispensed bottle.
Cipla Limited is recalling 4,800 bottles of Nevirapine Extended Release Tablets, 400 mg, because they failed to meet dissolution specifications.
Cardinal Health is recalling Protexis Neoprene Surgical Gloves because the packaging contains incorrect breakthrough times for specific chemotherapy drugs.
Cardinal Health is recalling Protexis Neoprene Surgical Gloves because the primary packaging contains incorrect breakthrough times for specific chemotherapy drugs.
Diagnostica Stago is recalling Staclot LA 20 test kits because some results showed shortened times outside the expected range.
Advanced Instruments, LLC is recalling GloCyte RBC Reagent because high fluorescent counts cause quality control checks to fail, preventing patient sample testing.
Cardinal Health 200, LLC is recalling Protexis Neoprene Surgical Gloves because the primary packaging contains incorrect breakthrough times for specific chemotherapy drugs.
Cardinal Health is recalling Protexis Neoprene Surgical Gloves because the packaging lists incorrect breakthrough times for specific chemotherapy drugs.
COVIDIEN LLC is recalling 32,071 units of 8Fr Argyle Suction Catheter Kits with Chimney Valve, Model 36826, because they were distributed while subject to importation refusal.
Cardinal Health 200, LLC is recalling Protexis Neoprene Surgical Gloves because the primary packaging contains incorrect breakthrough times for specific chemotherapy drugs.
Cardinal Health 200, LLC is recalling Protexis Neoprene Surgical Gloves because the packaging contains incorrect breakthrough times for specific chemotherapy drugs.
Ortho-Clinical Diagnostics is recalling 728 VITROS 4600 Chemistry Systems because a software anomaly may incorrectly extend reagent stability time.
Cardinal Health 200, LLC is recalling Protexis Neoprene Surgical Gloves because the primary packaging contains incorrect breakthrough times for specific chemotherapy drugs.
Zimmer Biomet is correcting the surgical technique for the Compress System to update selection criteria for anti-rotation pin placement.
Glenmark Pharmaceuticals is recalling 5,016 blister packs of Aprepitant 40 mg capsules because some packs are missing capsules.
VistaPharm is recalling Nystatin Oral Suspension because it failed impurity specifications. The affected product is distributed nationwide and in Puerto Rico.
Prevost is recalling 676 buses because a steering component may fracture, causing a loss of steering and increasing crash risk.
Daimler Trucks is recalling 2019-2020 Thomas Built Saf-T-Liner C2 school buses because an electrical overload may cause the engine to shut down, increasing crash risk.
Collins Bus Corporation is recalling 2018 SH, DH, P24, T22, T24, and TH buses because seat bolts may not be properly tightened, increasing injury risk in a crash.
Jennie-O is recalling approximately 164,210 pounds of raw ground turkey products produced in October 2018 due to possible Salmonella Reading contamination.
Daimler Trucks North America is recalling 2019-2020 Thomas Built Saf-T-Liner C2 buses because an electrical overload may cause the engine to shut down, increasing crash risk.
Harley-Davidson is recalling 2016-2019 Street 500, 750, and 750A motorcycles because brake calipers may corrode internally, causing increased brake drag and a higher risk of crash.
PACCAR is recalling 25,556 Kenworth and Peterbilt trucks because a clutch component may fail, causing unintended vehicle movement.
Nissan is recalling 23,903 2019 Altima vehicles because a fuel tube retainer clip may not be locked, risking fuel leaks, fires, or engine stalling.
Honda is recalling 2017-2018 Clarity Fuel Cell vehicles previously repaired under recall 18V-068 because incomplete software updates may cause partial or complete power loss.