Health product recall

MAGNETOM Flow.Ace

Last updated

Summary

Product
MAGNETOM Flow.Ace
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

MAGNETOM Flow.Ace

218718

11571247

Issue

Siemens Healthineers is advising customers of a software issue affecting syngo.via MR Cardiac Analysis MR
Flow Quantification when used with Beat Sensor triggering for retrospectively gated 2D cardiac flow
examinations.
The issue affects the MAGNETOM MR scanner model MAGNETOM Flow.Ace when operated with one of the
software versions and both licenses specified as follows :
. Software Versions Numaris/X VA51A, VA60A, VA61A, VA70A, VB10A, VB20A/NX2510;
. Beat Sensor / Pilot Tone Cardiac License (11344791) and
. syngo.via MR Cardiac Analysis MR Flow Quantification License (7106227 or 11344838)

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Siemens Shenzhen Magnetic Resonance Ltd.

Siemens Mri Center, Shenzhen, China, 518057

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82919

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