Hazard
135 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all unapproved device recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Get Tested International AB is recalling 13 units of its Iodine Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 2 units of its Gut Microbiome Test Mega because the product was distributed without premarket approval or clearance.
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 47 units of its Blood Type 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.
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 4 units of its MPOX 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 40 units of its Urinary Tract Infection Test 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 94 units of its Parasite Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 5 units of its Chlamydia 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 48 units of its Diabetes Test (ketones & glucose) 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 16 units of its Allergy & Food Intolerance 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.
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 10 units of its Vitamin D2 and D3 Test 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 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 1 unit of its Alcohol (ALC) Test Saliva 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.
ReQuest Measles IgM ELISA kits, catalog number 01-190M, are recalled because the test kit lacks premarket approval or clearance. 376 kits are affected.