Public recall detail

Siemens Healthcare GmbH Magnetom Systems

2026-10-27

medium
Health products Health product recall
Quick summary

Quick summary: Siemens Healthcare GmbH Magnetom Systems. Reason: Health product recall. Category: Health products. Date: 2026-10-27.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Siemens Healthcare GmbH Magnetom Systems. Reason: Health product recall. Category: Health products. Date: 2026-10-27.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandSiemens Healthcare Gmbh
ProductSiemens Healthcare GmbH Magnetom Systems
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82865

Affected products

ProductMagnetom Prisma
LotNot applicable.
Model10849582
Serial numberNot applicable.
DescriptionMagnetom Prisma
ProductMagnetom Aera
LotNot applicable.
Model10432914
Serial numberNot applicable.
DescriptionMagnetom Aera
ProductMagnetom Skyra
LotNot applicable.
Model10432915
Serial numberNot applicable.
DescriptionMagnetom Skyra
ProductManetom Prisma Fit
LotNot applicable.
Model10849583
Serial numberNot applicable.
DescriptionManetom Prisma Fit
ProductMagnetom Terra.X
LotNot applicable.
Model11371478
Serial numberNot applicable.
DescriptionMagnetom Terra.X
ProductMagnetom Terra.X
LotNot applicable.
Model11371477
Serial numberNot applicable.
DescriptionMagnetom Terra.X

Issue

The service pack NX VA60A-SP04 is a bug fix update (full installation) that solves/improves the following: Latest it security deliveries and increase in overall stability (syngo MR XA60A-SD12 content included) Installation of multiple SW delta packages now possible at the same time EU DataAact (EY) 2023/2854 implementation:access to all machine data Solved image loading errors for MR Breast Biopsy General MR Protocol Manager improvements Coil specifications adjusted for BM Body 18 Pilot Tone and Spine 32 and 1.5T Sentinelle Breast coils image brightness Supporting IEC 60601-1 compliance, enabling predictable and safe system behavior with regard to table movement

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Radiology
CompaniesSiemens Healthcare Gmbh Henkestr. 127, Erlangen, Germany, 91052
Recall date2026-10-20
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82865
Background{}
CompaniesSiemens Healthcare Gmbh Henkestr. 127, Erlangen, Germany, 91052
AudiencesHealthcare
Source updated2026-10-27

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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