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FDAApril 26, 2024device

CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The H5b component may fail to amplify, resulting in an inconclusive result.

What to do

FDA enforcement status: Terminated

Brands named

centers for disease control and preventioncenterscenters for

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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