Siemens recalls MAGNETOM Aera MRI devices with model #10432914 due to potential open port in quench venting system when using optional horizontal outlet. Affected units may require repair or replacement.
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 Aera MRI machines with model number 10432914 because a potential open port in the quench venting system could cause issues when using the optional horizontal outlet. This recall matters because it addresses a safety concern that could lead to equipment malfunction.
The quench venting system is designed to safely release helium gas from the MRI machine. If an open port exists in this system when using the optional horizontal outlet, it could lead to improper gas release and potential equipment malfunction.
Medical facilities using Siemens MAGNETOM Aera MRI machines with model #10432914 are likely affected. Staff and patients using the optional horizontal outlet on the quench line assembly are at the highest risk.
Check for model number 10432914 on the device. Serial numbers include a long list of numbers starting with 41878 and ending with 42533. The affected units were sold with the optional horizontal outlet on the quench line assembly.
Look for model number 10432914 on the device to confirm if it is affected.
Reach out to Siemens Medical Solutions USA, Inc for guidance on next steps and potential repairs.
The recall is due to a potential open port in the quench venting system when using the optional horizontal outlet on the quench line assembly, which could lead to equipment malfunction.
No, the recall does not require immediate discontinuation of use. Affected units may need repair or replacement.
Check for model number 10432914 and serial numbers starting with 41878 and ending with 42533. The device must have the optional horizontal outlet on the quench line assembly.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2342-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2342-2019 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.
