Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:15342
Brand Name:GE CardiacVX and CardiacVX Flow Analysis software
Model:
Affected:Version: 1.1.0 Ext.D
Software version:
Recalling Organisation:GE Healthcare Limited
Level 7, Vero Centre
48 Shortland St
Auckland 1010
Contact Information:0800 659 465
Manufacturer:GE Medical Systems SCS
Issue:CardiacVX and CardiacVX Flow report higher than actual flow values on phase-contrast images acquired with magnitude weighting mask enabled. Note that this issue can only occur on phase-contrast MR protocols with the magnitude weighting mask option enabled.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:9/9/2013
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