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Medical Device

Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485

Recall date: 2026-05-13 · Source: FDA_DEVICE
Product
Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485
Reason for recall
Respiratory/sore throat panel test may result in false negative results and control failures.
Units affected
2400 pouches
Description
Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485
View official recall notice →