FDAApril 28, 2025device

Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the qualitative detection and differentiation of RNA from influenza A virus (flu A), influenza B virus (flu B), Respiratory...

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

The hazard

There were reports of an increase in reactive negative controls and false positive results.

What to do

FDA enforcement status: Ongoing

Brands named

abbott molecularabbott

UPCs

00884999049338

Recall history

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

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