TeraRecon Aquarius iNtuition Client Viewer recall — FDA Z-1070-2015
Software anomaly related to RECIST1.1 target lesion evaluation criteria in Findings Workflow Module within the Aquarius iNtuition Client Viewer.
Overview of recall records associated with TeraRecon, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Software anomaly related to RECIST1.1 target lesion evaluation criteria in Findings Workflow Module within the Aquarius iNtuition Client Viewer.
This page summarizes recall records in which the official source identifies TeraRecon, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.