Medical Device Recall: Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant Assay, Rubeola IgM Model/Catalog Number: 01-190M Software Version: N/A Product Description: Measles IgM tests, performed
Quest International, Inc. · July 17, 2025
Reason for Recall
Measles IgM Test Kit lacks premarket approval or clearance.
Product Description
Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant Assay, Rubeola IgM Model/Catalog Number: 01-190M Software Version: N/A Product Description: Measles IgM tests, performed using ELISA (Enzyme-Linked Immunosorbent Assay) method, used to detect the presence of IgM antibodies against measles virus in a patient's serum or plasma Component: not a component
Distribution
US Nationwide distribution in the states of Utah, Texas, and Arizona.
States Affected
NATIONWIDE
Quantity Affected
376 kits
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2552-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.