FDAJanuary 22, 2020device

FilmArray BCID Panel, RFIT-ASY-0127, 6, Rx Only, CE, IVD, UDI: 00815381020093 used with the following BACT/ALERT Blood Culture Bottle Catalog No./Description: 410851/BACT/ALERT¿ FA Plus 410852/BACT/ALERT¿ FN Plus 410853/BACT/ALERT¿ PF Plus 259790/BACT/ALERT¿ SN Product Usage: is a qualitative mul...

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

The hazard

There is an increased risk of false positive Proteus results when using the Film Array Blood Culture Identification Panel (BCID) in vitro diagnostic test of blood cultures used in conjunction with specific media types. False positive Proteus results from this test may lead to patients receiving improper antibiotic treatment until culture results are available (within 24-48 hours).

What to do

FDA enforcement status: Terminated

Brands named

biofire diagnosticsbiofire

UPCs

00815381020093

Recall history

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

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