FDAApril 22, 2015device

Alere i Influenza A & B Product Usage: The Alere i Influenza A and B assay, performed on the Alere i Instrument, is a rapid molecular in vitro diagnostic test utilizing an isothermal nucleic acid amplification technology for the qualitative detection and discrimination of influenza A and B viral ...

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

The hazard

High invalid rate and an increased risk of false negative results with certain lots of the Alere i Influenza A & B kit.

What to do

FDA enforcement status: Terminated

Brands named

alere scarborough inc dba binaxalerealere scarborough

Recall history

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

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