FDAApril 8, 2021device

Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) qualitative test run on the Revogene¿ instrument for the detection of SARS-CoV-2 nucleic acid from nasopharyngeal swab (NPS) specimens from individuals suspected of COVID-19

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

The hazard

Emergency Use Application (EUA) application withdrawn as false negative results reported

What to do

FDA enforcement status: Terminated

Brands named

meridian biosciencemeridian

Recall history

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

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