Siemens MAGNETOM Spectra MRI: Open Quench Port Risk

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Contact the company & request your remedy

Recalling firmSiemens Medical Solutions USA, Inc40 Liberty Blvd, N/A · Malvern, PA 19355-1418

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Siemens is recalling MAGNETOM Spectra MRI machines with model number 10837643 because of a potential open port in the quench venting system when using the optional horizontal outlet. This could lead to safety issues if the port is not properly sealed.

Why it’s dangerous

The quench venting system is designed to safely release helium gas from the MRI machine. If the port is open when using the optional horizontal outlet, it could allow helium to escape, potentially causing a safety hazard.

Who’s affected

MAGNETOM Spectra MRI machines with model number 10837643 and serial numbers 72030 or 72023 are affected. Medical facilities using these devices are most at risk.

How to tell if you have this one

Check for model number 10837643 and serial numbers 72030 or 72023 on the device. These specific models and serial numbers are part of the recall.

Brand
Siemens
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Model Number
Look for model number 10837643 on the device.
Contact Manufacturer
Contact Siemens Medical Solutions USA, Inc for further instructions.

✎ GovInfoNow

Questions people ask

Is this recall dangerous?

The recall describes a potential open port in the quench venting system, but the exact risk level is not specified in the record.

What should I do if I have this model?

Check the model number and serial number on the device. Contact Siemens Medical Solutions USA, Inc for further instructions.

How can I tell if my device is affected?

Devices with model number 10837643 and serial numbers 72030 or 72023 are affected.

Take action

Contact Siemens

We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2344-2019 — Siemens Siemens

Hello,

I own a Siemens that is covered by recall Z-2344-2019 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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Where this comes from

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.

Official source: FDA Recall #Z-2344-2019 (July 9, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2344-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Siemens Medical Solutions USA, Inc recalls MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643

Recall notice