Ventana Image Analysis System (VIAS) - PATHWAY anti-HER-2/neu (4B5) primary antibody with software version 2.3.0.2, Model Number: VIAS-799-10000-00, Pathology Image Analysis System, Ventana Medical Systems, Inc., Tucson, AZ 85755
FDA Recall Z-0571-2008 · Posted 2008-03-18
Recalling FirmVentana Medical Systems Inc
Recall StatusTerminated
Product CodeNQN
Date Initiated2007-06-26
Date Terminated2012-03-26
Product Quantity77 devices
Reason for Recall
Incomplete upgrade: The software upgrade from February 1, 2007 may not have been
completed. This software upgrade adds the algorithm (Slidetype) for the
PATHWAY anti-HER-2/neu (4B5) antibody to the VIAS system.
Firm Action
Beginning in 6/07, Ventana Medical Systems, Inc., made phonecalls to labs asking to confirm software version, date of upgrade if available and confirmation of whether site uses 4B5 and Imaging together. A phone script was provided. Customers with systems not ugraded were to upgrade before further use of system. A notification letter dated 8/17/2007 was later sent to VIAS customers advising that the software upgrade from February 1 , 2007 may not have been
completed on their system. This software upgrade adds the algorithm (Slidetype) for the
PATWAY anti-HER-2/neu (4B5) antibody to their VIAS system . This Slidetype is cleared for marketing
and is required prior to imaging slides stained with PATHWAY anti-HER-2/neu (4B5).
The letter also advises that their VIAS and NEXES systems are conneded to the internet which enables this upgrade to be
performed remotely with the support of the Ventana Medical Systems Customer Support Center
(CSC). customers are instructed to call the CSC to carry out the upgrade or to schedule a
Technical Applications Specialist (TAS) to assist with the upgrade in their lab. Arrangements for the upgrade are to be made prior to imaging slides stained with PATHWAY
anti-HER-2/neu (4B5).
Root Cause
Software change control
Distribution Pattern
Nationwide and Canada
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.