Siemens recalls MAGNETOM Verio Dot Upgrade MRI machines with model 10684334 due to potential ice blockage in helium venting system, risking pressure build-up and helium leaks.
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 Verio Dot Upgrade 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 helium venting system can prevent helium gas from escaping during a quench event. This may cause pressure to build up inside the helium containment system, potentially rupturing it and leaking helium into the scanning room.
Medical facilities using the recalled MAGNETOM Verio Dot Upgrade MRI machines with model number 10684334 are most at risk. Patients and staff in these facilities could be exposed to helium leaks if the hazard occurs.
Check for model number 10684334 on the device. The UDI numbers listed in the recall include specific sequences starting with (01)04056869006680(21) followed by numbers. Serial numbers are listed in the recall.
Identify the model number on the device to confirm if it matches 10684334.
Reach out to Siemens Medical Solutions USA, Inc for further instructions on the recall.
The model number is 10684334.
Check for model number 10684334 or the UDI numbers listed in the recall, which include specific sequences starting with (01)04056869006680(21).
The recall does not specify a remedy, so contact Siemens Medical Solutions USA, Inc for further instructions.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2666-2025 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2666-2025 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.
