Siemens recalls MAGNETOM Skyra MRI models with serial numbers starting 46066-46298 for potential open port in quench venting system. Affected units may require repair to prevent safety issues.
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Siemens is recalling MAGNETOM Skyra MRI machines with specific serial numbers due to a potential open port in the quench venting system. This could lead to safety risks if the device is used improperly.
The quench venting system is designed to safely release helium gas from the MRI machine. An open port could allow helium to escape improperly, potentially causing safety hazards during operation.
Medical facilities using Siemens MAGNETOM Skyra MRI machines with the listed serial numbers are most at risk. Patients and staff could face safety issues if the device malfunctions.
Check the serial number on your MAGNETOM Skyra MRI machine. The affected units have serial numbers starting with 46066 through 46298 as listed in the recall notice.
Identify the serial number on your MAGNETOM Skyra MRI machine to determine if it is affected.
Reach out to Siemens Medical Solutions USA, Inc. for guidance on next steps and potential repairs.
The quench venting system may have an open port when using the optional horizontal outlet on the quench line assembly, which could lead to safety risks.
Check the serial number on your MAGNETOM Skyra MRI machine. Affected units have serial numbers starting with 46066 through 46298 as listed in the recall notice.
No, but you should contact Siemens for guidance as the hazard requires specific attention to prevent safety issues.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2343-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2343-2019 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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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.
