Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:29332
Brand Name:VITEK 2 SYSTEMS SOFTWARE
Model:
Affected:Reference Number AST - ST03 Product Name 421040 and Reference Number AST - YS08 Product Name 420739
Software version:
Recalling Organisation:Medi'Ray New Zealand Ltd
53-55 Paul Matthews Road
Albany
Auckland 0632
Contact Information:0800 633 472
Manufacturer:BioMerieux Inc
Issue:During a historical review of VITEK 2 Systems software BIOART rules, bioMérieux has identified five (5) BIOART rule discrepancies. Potential impact of the discrepancies at your facility is dependent upon the breakpoint (BP) set in use and the AST card types being utilized.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:2/5/2022
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