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Official recall record

MAGNETOM Prisma, Vida, Skyra, Verio Systems

Health Canada — Medical Devices · 2025-08-27 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-08-27
Last updated (per notice)
2025-11-18
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

This field safety corrective action addresses a potential safety issue associated with the magnet venting paths of some 3 Tesla MRI systems, which will require on-site inspection. An ice blockage may have built up within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed vent paths, leading to a pressure build-up in the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room. Recall start date: August 14, 2025

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 2026-05-31.

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ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.