State
72,940 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,723 recalls whose distribution notice names Kansas specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Get Tested International AB is recalling 184 units of its Menopause (FSH) 2 Tests because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 2043 units of its 8 in 1 STI Test Kit because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 33000 containers of Globe Zinc Oxide Ointment USP over current good manufacturing practice deviations.
Blossom Pharmaceuticals is recalling 912 containers of Nivagen Zinc Oxide Ointment USP 20%, 15 oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 5 units of its Food Intolerance Test Small because the product was distributed without premarket approval or clearance.
Siemens Medical Solutions USA is recalling 6 MAMMOMAT Inspiration systems because operator tables were sold together with a bus-installation kit they are not released for.
Get Tested International AB is recalling 148 units of its Diabetes HbA1c Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 94 units of its Parasite Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 24 units of its Akkermansia Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 16 units of its Food Intolerance Test Medium because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 4 units of its Continuous Glucose Monitor (CGM) because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 18 units of its Neurotransmitters Plus because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 17 units of its Adrenal Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 17 units of its DHEA Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 6 units of its Food Intolerance Test Large because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 8 units of its IBS Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its Food Sensitivity Test Large because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 12 units of its Peptic Ulcer Test (H. pylori) because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 10 units of its Men's Hormone Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 4 units of its MPOX Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1 unit of its Food Sensitivity Test Medium because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 4 units of its Organic acids Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its GI Microbiome Profile XL because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 45 units of its Intestinal Worms Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1 unit of its Drug Test Small (4 substances) because the product was distributed without premarket approval or clearance.