FDADecember 5, 2025device

Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300

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

The hazard

The affected lots show a decline in performance over time, which may lead to false-negative results.

What to do

FDA enforcement status: Ongoing

Brands named

meridian biosciencemeridian

UPCs

00840733102349

Recall history

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

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Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300 — Recall Details · AllClear