FDAApril 22, 2026device

BioFire Joint Infection (JI) Panel REF: RFIT-ASY-0138, 30 test Kit.

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

The hazard

Contamination to in-vitro diagnostic test may result in false positives.

What to do

FDA enforcement status: Ongoing

Brands named

biofire diagnosticsbiofire

UPCs

00815381020192

Recall history

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

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