FDANovember 13, 2018device

VITEK¿ 2 Systems Software Version 9.01 Update Kit.

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

The hazard

The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect organism identification information as well as the associated Antimicrobial Susceptibility Testing (AST) results when using the VITEK¿ 2 FLEXPREP" feature.

What to do

FDA enforcement status: Terminated

Brands named

biomerieux

UPCs

03573026561260

Recall history

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

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