Class II
Medical Device Recall: CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
Centers For Disease Control and Prevention · April 26, 2024
Reason for Recall
The H5b component may fail to amplify, resulting in an inconclusive result.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
191 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2220-2024
Status: terminated
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.