FDAFebruary 15, 2022device

Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded Revogene: Catalog Number 610210 GenePOC branded Revogene: Catalog Number 130840

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

The hazard

The photomultiplier tube, may have compromised functionality in some instruments. As a result, the user is likely to observe an increase in false-positive or indeterminate results.

What to do

FDA enforcement status: Ongoing

Brands named

meridian biosciencemeridian

UPCs

00840733102318

Recall history

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

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Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded Revogene: Catalog Number 610210 GenePOC branded Revogene: Catalog Number 130840 — Recall Details · AllClear