Siemens recalls specific model X-ray machines due to power supply tolerance issues that can prevent X-ray function during procedures. Affected units may require repair or replacement.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
Siemens is recalling certain AXIOM Artis MP X-ray machines because a power supply issue can cause the X-ray tube to stop working during procedures. This could lead to failed imaging and potential delays in medical care.
The power supply has a tolerance issue that can cause generator A100 failure when voltage exceeds a specific threshold. This prevents the X-ray tube from receiving required voltage, making X-ray imaging impossible during procedures.
Medical facilities using the recalled model number 5904466 X-ray machines are affected. Patients undergoing procedures with these machines may face delayed imaging.
Check for the model number 5904466 on the machine. Serial numbers listed in the recall include 20334, 20052, 20303, and other numbers provided in the recall notice.
Reach out to Siemens Medical Solutions USA, Inc. for guidance on next steps for affected units.
The power supply has a tolerance issue that can cause generator A100 failure, preventing X-ray tube from receiving required voltage during procedures.
Model number 5904466 with specific serial numbers listed in the recall notice.
No, but affected units may require repair or replacement to ensure X-ray function during procedures.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2014-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2014-2019 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.
