State
72,969 recalls have nationwide distribution and so reach Wyoming. 3,219 additional recalls listed Wyoming specifically in their distribution scope.
Of the 3,219 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 543 (17%) are Severe.
Which agencies issued them
These figures cover only the 3,219 recalls whose distribution notice names Wyoming specifically. The 72,969 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 10 units of its Vitamin D2 and D3 Test because the product was distributed without premarket approval or clearance.
Philips Ultrasound is recalling 4,819 Lumify Diagnostic Ultrasound Systems because compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imaging.
Teva Pharmaceuticals USA is recalling 15,944 cartons of Testosterone Gel 1% unit-dose packets because a defect in the side-seal allows leakage of product.
Get Tested International AB is recalling 100 units of its Kidney 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 60 units of its Trichomonas Vaginalis test 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 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 Biological Age & Longevity 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 258 units of its HPV Antigen 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 12 units of its Melatonin 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 8 units of its Fructose Intolerance Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1218 units of its D-Dimer Test 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 76 units of its Allergy test Small because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 115 units of its Iron Deficiency Test (ferritin) because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 10 units of its Pollen Allergy Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 4 units of its Gut Microbiome Test XL because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 1,560 containers of Dynashield Skin Protectant, 16 oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 463 units of its Gonorrhea test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 29 units of its Pet Allergy 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.