CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
Reported: July 3, 2024 Initiated: April 26, 2024 #Z-2220-2024
Product Description
CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
Reason for Recall
The H5b component may fail to amplify, resulting in an inconclusive result.
Details
- Recalling Firm
- Centers For Disease Control and Prevention
- Units Affected
- 191 units
- Distribution
- US Nationwide distribution.
- Location
- Atlanta, GA
Frequently Asked Questions
What product was recalled? ▼
CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11. Recalled by Centers For Disease Control and Prevention. Units affected: 191 units.
Why was this product recalled? ▼
The H5b component may fail to amplify, resulting in an inconclusive result.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 3, 2024. Severity: Moderate. Recall number: Z-2220-2024.
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