Public recall detail

Magnetom Scanner

2026-10-28

medium
Health products Health product recall
Quick summary

Quick summary: Magnetom Scanner. Reason: Health product recall. Category: Health products. Date: 2026-10-28.

Recommended action

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

Recall details

Quick summary: Magnetom Scanner. Reason: Health product recall. Category: Health products. Date: 2026-10-28.

Official details

Affected product details

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

BrandSiemens Healthineers Ag
ProductMagnetom Scanner
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82871

Affected products

ProductMagnetom Scanner
LotMore than 10 numbers, contact manufacturer.
Model11060815
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionMagnetom Scanner
ProductMagnetom Scanner
Lot196408
Model11344916
Serial number196408
DescriptionMagnetom Scanner
ProductMagnetom Scanner
Lot196427
Model11344916
Serial number196427
DescriptionMagnetom Scanner
ProductMagnetom Scanner
Lot196822
Model11344916
Serial number196822
DescriptionMagnetom Scanner
ProductMagnetom Scanner
Lot196406
Model11344916
Serial number196406
DescriptionMagnetom Scanner
ProductMagnetom Scanner
Lot196680
Model11344916
Serial number196680
DescriptionMagnetom Scanner

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 Healthineers Ag Siemensstr. 3, Forchheim, Germany, 91301
Recall date2026-10-20
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82871
Background{}
CompaniesSiemens Healthineers Ag Siemensstr. 3, Forchheim, Germany, 91301
AudiencesHealthcare
Source updated2026-10-28

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

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