Siemens recalls MAGNETOM Skyra fit MRI machines with model 10849580 due to potential ice blockage in helium venting system, risking pressure buildup and helium leaks during quench events.
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 models of MAGNETOM Skyra fit MRI machines because ice can block the helium venting system. If a quench occurs, this could cause pressure buildup and helium leaks into the scanning room.
Ice blockages in the magnet venting system could prevent helium gas from escaping during a quench event. This may cause pressure buildup in the helium containment system, potentially rupturing it and leaking helium into the scanning room.
Owners of MAGNETOM Skyra fit MRI machines with model number 10849580 are affected. Medical facilities using these machines are most at risk due to potential helium leaks during quench events.
Check for model number 10849580 on the machine. Look for specific UDI numbers or serial numbers listed in the recall notice, including those added after February 2026.
Identify the model number on your MAGNETOM Skyra fit machine to confirm if it's affected.
Reach out to Siemens Medical Solutions USA, Inc for further instructions on the recall.
Model number 10849580 with specific UDI and serial numbers listed in the recall notice.
The recall notice does not specify a fix; affected owners should contact Siemens for instructions.
The recall does not describe how to detect ice blockage; it only states the potential risk.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2661-2025 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2661-2025 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.
