Siemens recalls MAGNETOM Vida (DE) MRI machines with model number 11060815 due to potential ice blockage in magnet venting system that could cause helium pressure build-up and rupture, leading to helium leaks in scanning rooms.
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.
Siemens is recalling specific MAGNETOM Vida MRI machines (model 11060815) because ice can block the magnet venting system. If a quench occurs (a sudden loss of superconductivity), helium gas may not escape properly, causing pressure buildup that could rupture the helium containment system and leak helium into the scanning room. This is a serious risk for MRI facilities using these machines.
Ice can form or block the magnet venting system. During a quench (when the superconducting magnet loses its superconductivity), helium gas normally escapes through designed venting paths. If blocked, pressure builds up in the helium containment system, which could rupture and release helium into the scanning room.
MRI facility staff and patients using the recalled MAGNETOM Vida (DE) MRI machines with model number 11060815. The risk is highest for facilities that operate these machines regularly.
Check if your MAGNETOM Vida (DE) MRI has model number 11060815. The product is identified by UDI numbers starting with (01)04056869039176 followed by specific serial numbers listed in the recall notice.
Verify your MAGNETOM Vida (DE) MRI has model number 11060815 by checking the label on the machine.
Reach out to Siemens Medical Solutions USA, Inc. for guidance on next steps if you have the recalled model.
Check if your MAGNETOM Vida (DE) MRI has model number 11060815. The recall applies to specific machines with this model number and associated UDI numbers.
Contact Siemens Medical Solutions USA, Inc. directly to confirm if your machine is affected and get instructions.
The recall describes a potential risk of helium leakage during a quench event, but no injuries have been reported specifically from this issue.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2667-2025 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2667-2025 from Siemens. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
