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BioFire Diagnostics

MedTech Current publications and recall entries tagged BioFire Diagnostics.

Device RecallsFDA Class II Recall Watch: 9–15 August 2026

BioFire recalls specified BIOFIRE RP2.1 lot after false-negative results

False-negative molecular respiratory results can directly affect diagnostic decision-making, making this recall particularly relevant to laboratories and IVD manufacturers. The failure also shows how a reagent-manufacturing error can escape normal controls while control assays still pass, creating a significant result-integrity and quality-system lesson.