FDAFDA · Food and drugs·Recall number Z-2220-2024
CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
Published July 3, 2024 · Recall initiated: April 26, 2024
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The H5b component may fail to amplify, resulting in an inconclusive result.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Centers For Disease Control and Prevention
- Distributor
- US Nationwide distribution.
- Lot
- Lot Code: Catalog # FluIVD03-11, lot 220307
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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