Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:24347
Brand Name:syngo.via CT apps
Model: syngo.CT Cardiac Function used in syngo.via VA20A, VA30A oder VB10A AND syngo.CT Cardiac Planning used in syngo.via VB20A oder VB30A
Affected:
Software version:
Recalling Organisation:Siemens Healthcare (NZ) Ltd
Millennium Centre, Part Level 2, Building A
600 Great South Road
Ellerslie
AUCKLAND 1051
Contact Information:0800 310 300
Manufacturer:Siemens Healthcare GmbH
Issue: There is a potential risk of a wrong measurement in the annulus plane during a TAVI planning procedure using syngo.CT Cardiac Function or syngo.CT Cardiac Planning.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:22/3/2019
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