FDAApril 1, 2026device

Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485

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

The hazard

Respiratory/sore throat panel test may result in false negative results and control failures.

What to do

FDA enforcement status: Ongoing

Brands named

biofire diagnosticsbiofire

UPCs

00815381020390

Recall history

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

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