State
72,940 recalls have nationwide distribution and so reach Wisconsin. 8,408 additional recalls listed Wisconsin specifically in their distribution scope.
Of the 8,408 recalls naming Wisconsin we have scored against our rubric, 1,547 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,957 (23%) are Severe.
Which agencies issued them
These figures cover only the 8,408 recalls whose distribution notice names Wisconsin 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 8 units of its Fructose Intolerance Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1210 units of its 3 in 1 STI Test because the product was distributed without premarket approval or clearance.
Philips North America is recalling 2,341 Incisive CT systems because a tube heat exchanger whose screws are not tightened after replacement may detach and damage other components.
Get Tested International AB is recalling 1 unit of its Sperm Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 9 units of its Estrogen & Progesterone Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 5187 units of its Iron Deficiency Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 35 units of its Fecal Occult Blood Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1557 units of its Vitamin D-Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 4081 units of its Epstein-Barr Virus (EBV VCA & EBNA IgG) Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 2 units of its Mycotoxin Panel Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 258 units of its HPV Antigen Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 2,592 bottles of WeCare Zinc Oxide Ointment, 15 oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 109 units of its Candida Test 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 6 units of its Gut Microbiome Test Small 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.
Get Tested International AB is recalling 5 units of its Food Intolerance Test Small because the product was distributed without premarket approval or clearance.
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 2043 units of its 8 in 1 STI Test Kit 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 1 unit of its Alcohol (ALC) Test Saliva because the product was distributed without premarket approval or clearance.
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 1 unit of its Organic Acids Profile Test Large because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 16 units of its Allergy & Food Intolerance 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.