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

> recall · VERIFIED · 2026-04-22

Firm: BioFire Diagnostics, LLC · Class II · Contamination to in-vitro diagnostic test   may result in false positives.

- Company: BioFire Diagnostics, LLC
- Sector: diagnostics
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED.