Official recall record

MAGNETOM Flow.Ace

Health Canada — Medical Devices · 2026-11-05 · CanadaType II

Issuing authority: Health Canada — Medical Devices
Published: 2026-11-05
Country of alert: Canada
Alert level: Type II
Alert type: recall

What the authority reported

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)

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-11-13.

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