Health & Personal Care
HIGH
FDA DEVICE
Quest International Measles IgM 01-190M Recall for False Premarket Clearance
Quest International recalls 376 Measles IgM ELISA kits nationwide in Utah, Texas and Arizona after discovering the product lacks premarket approval or clearance. The high-risk health device carries a Class II designation. Stop using the device immediately and follow manufacturer recall instructions.
Quest International
Measles IgM