Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0451-2024 — BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls, Inc (MMQCI) FilmArray BCID2 Control Panel M416, which is referenced in Quality Control Materials for use with BIOFIRE FILMARRAY and BIOFIRE SPOTFIRE Panels - FLM1-PRT-0251

U.S. FDA — Device Enforcement · United States · 2023-10-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0451-2024
Date of alert
2023-10-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
BioFire Diagnostics, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00815381020338
Reported risk: Routine quality control testing of affected blood culture identification panel with affected control panel may need to be amended, due to control panel/instrument characteristic changes, that lead C. tropicalis to be amplified in some portion of test runs, but then it's reported as "Not Detected" because the assay amplicon Tm is outside the acceptable limit assigned for calling positive results.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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