Quick summary: MAGNETOM Flow.Ace. Reason: Health product recall. Category: Health products. Date: 2026-11-05.
MAGNETOM Flow.Ace
2026-11-05
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: MAGNETOM Flow.Ace. Reason: Health product recall. Category: Health products. Date: 2026-11-05.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
Issue
Siemens Healthineers is advising customers of a software issue affecting syngo.via MR Cardiac Analysis MRFlow Quantification when used with Beat Sensor triggering for retrospectively gated 2D cardiac flowexaminations.The issue affects the MAGNETOM MR scanner model MAGNETOM Flow.Ace when operated with one of thesoftware 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 you should do
- Contact the manufacturer if you require additional information.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
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