Centers For Disease Control and Prevention: Device Recall
Recall #Z-2220-2024 · 04/26/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2220-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Centers For Disease Control and Prevention
- Status
- Terminated
- Date Initiated
- 04/26/2024
- Location
- Atlanta, GA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 191 units
Reason for Recall
The H5b component may fail to amplify, resulting in an inconclusive result.
Product Description
CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
Distribution Pattern
US Nationwide distribution.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.