bioMerieux, Inc. recalls VITEK¿ 2 Systems Software Version 9.01 Update Kit.
Recalled Product
VITEK¿ 2 Systems Software Version 9.01 Update Kit.
Hazard / Issue
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.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Product Description: KIT UPDT VTK2 9.01 EN, UDI: 03573026561260
View official government recall
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