Official recall record

MAGNETOM Vida Fit. Model Number: 11410481.

US FDA — Medical Devices · 2025-08-28 · United StatesClass I

Issuing authority: US FDA — Medical Devices
Recall initiated by firm: 2025-08-28
Country of alert: United States
Alert level: Class I
Alert type: recall
Brand on record: Siemens Medical Solutions USA, Inc

What the authority reported

There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within 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.

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: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: US FDA — Medical Devices · United States · all filters

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All 23 official recall notices naming Siemens Medical Solutions USA, Inc on this site →

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.