State
72,940 recalls have nationwide distribution and so reach New York. 12,903 additional recalls listed New York specifically in their distribution scope.
Of the 12,903 recalls naming New York we have scored against our rubric, 1,501 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,134 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,903 recalls whose distribution notice names New York specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blossom Pharmaceuticals is recalling 8,184 bottles of Dynagel Moisturizing Wound Hydrogel over current good manufacturing practice deviations.
Get Tested International AB is recalling 18 units of its Neurotransmitters Plus 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 3 units of its Biological Age & Longevity 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 528 units of its Syphilis 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 1218 units of its D-Dimer Test 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 3 units of its Gut Microbiome Test Large 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 463 units of its Gonorrhea 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.
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 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 Sperm Test because the product was distributed without premarket approval or clearance.
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 1557 units of its Vitamin D-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 258 units of its HPV Antigen 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 4 units of its Gut Microbiome Test XL because the product was distributed without premarket approval or clearance.
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 8 units of its Fructose Intolerance Test 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.