State
72,940 recalls have nationwide distribution and so reach Ohio. 11,719 additional recalls listed Ohio specifically in their distribution scope.
Of the 11,719 recalls naming Ohio we have scored against our rubric, 2,106 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,413 (21%) are Severe.
Which agencies issued them
These figures cover only the 11,719 recalls whose distribution notice names Ohio 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 14 units of its Neurotransmitters XL because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 2400 containers of Wecare Calasoothe over current good manufacturing practice deviations.
Get Tested International AB is recalling 2 units of its Pregnancy 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.
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 37 units of its Women's Hormone Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 12150 bottles of Globe Clotrimazole Cream over current good manufacturing practice deviations.
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 12 units of its Serotonin Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 8,184 bottles of Dynagel Moisturizing Wound Hydrogel over current good manufacturing practice deviations.
Get Tested International AB is recalling 128 units of its Ovulation Test (5 tests) because the product was distributed without premarket approval or clearance.
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.
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.
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 35 units of its Fecal Occult Blood Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 31 units of its Leaky Gut Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its Food Sensitivity Test Small because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 47 units of its Blood Type 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.
Baxter Healthcare is recalling 118 Welch Allyn thigh replacement bladder kits because a kit may contain a Large Adult size bladder rather than a Thigh size bladder.
Get Tested International AB is recalling 658 units of its Parasite Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 18,912 containers of Wecare Enema, 4.5 Fl Oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 1 unit of its GI Microbiome Profile Small because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 13536 containers of Nivagen Zinc Oxide Ointment over current good manufacturing practice deviations.
Blossom Pharmaceuticals is recalling 9600 containers of Lanashield Skin Barrier over current good manufacturing practice deviations.