State
72,940 recalls have nationwide distribution and so reach Georgia. 9,588 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,588 recalls naming Georgia we have scored against our rubric, 1,464 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,164 (23%) are Severe.
Which agencies issued them
These figures cover only the 9,588 recalls whose distribution notice names Georgia 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 17 units of its Adrenal Test 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 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 3 units of its Food Sensitivity 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.
Blossom Pharmaceuticals is recalling 9600 containers of Lanashield Skin Barrier over current good manufacturing practice deviations.
Get Tested International AB is recalling 940 units of its Lyme Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 36 units of its NAD Profile Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 19 units of its Hair Mineral Analysis 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.
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 9 units of its Estrogen & Progesterone Test because the product was distributed without premarket approval or clearance.
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 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.
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.
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 1 unit of its Alcohol (ALC) Test Saliva 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 71 units of its Allergy Test IgE because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 14700 bottles of Globe Clotrimazole Cream USP over current good manufacturing practice deviations.
Get Tested International AB is recalling 4 units of its Continuous Glucose Monitor (CGM) 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.