State
72,966 recalls have nationwide distribution and so reach Michigan. 9,518 additional recalls listed Michigan specifically in their distribution scope.
Of the 9,518 recalls naming Michigan we have scored against our rubric, 1,556 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,145 (23%) are Severe.
Which agencies issued them
These figures cover only the 9,518 recalls whose distribution notice names Michigan specifically. The 72,966 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 60 units of its Trichomonas Vaginalis test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 33 units of its Sperm 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.
Get Tested International AB is recalling 19 units of its Allergy test Small 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 Food Sensitivity Test Medium because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 128 units of its Ovulation Test (5 tests) because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1361 units of its Herpes (HSV-1 & HSV-2) Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 12 units of its Serotonin Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 6 units of its Gut Microbiome Test Small because the product was distributed without premarket approval or clearance.
Siemens Medical Solutions USA is recalling one MAMMOMAT Fusion system because an operator table was sold together with a bus-installation kit it is not released for.
Get Tested International AB is recalling 71 units of its Allergy Test IgE because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 109 units of its Candida 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.
Fresenius Kabi USA is recalling 15,862 Ivenix Infusion System large volume pumps because downstream occlusion alarms may occur at low flow rates when a check valve is added to the administration set.
Get Tested International AB is recalling 27 units of its PSA Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 18 units of its Neurotransmitters Basic 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 94 units of its Parasite 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.
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 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 GI Microbiome Profile Small because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 658 units of its Parasite Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 184 units of its Menopause (FSH) 2 Tests because the product was distributed without premarket approval or clearance.