State
72,940 recalls have nationwide distribution and so reach Puerto Rico. 3,090 additional recalls listed Puerto Rico specifically in their distribution scope.
Of the 3,090 recalls naming Puerto Rico we have scored against our rubric, 366 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 625 (20%) are Severe.
Which agencies issued them
These figures cover only the 3,090 recalls whose distribution notice names Puerto Rico 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 1218 units of its D-Dimer Test 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 528 units of its Syphilis Test 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 36 units of its NAD Profile 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.
Get Tested International AB is recalling 19 units of its Hair Mineral Analysis 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 31 units of its Leaky Gut 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.
Blossom Pharmaceuticals is recalling 1,560 containers of Dynashield Skin Protectant, 16 oz, over current good manufacturing practice deviations.
Blossom Pharmaceuticals is recalling 9600 containers of Lanashield Skin Barrier over current good manufacturing practice deviations.
Get Tested International AB is recalling 17 units of its DHEA Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its Gut Microbiome Test Large because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 55 units of its SIBO 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 128 units of its Ovulation Test (5 tests) 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 1 unit of its Organic Acids Profile Test Large 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 24 units of its Akkermansia Test 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.
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.
Blossom Pharmaceuticals is recalling 7,920 bottles of Nivagen Zinc Oxide Ointment USP 20%, 1 oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 18 units of its Neurotransmitters Basic because the product was distributed without premarket approval or clearance.