Siemens recalls specific AXIOM Artis BA X-ray machines (model 5904656) due to power supply issues that can cause X-ray tube failure during procedures. Affected units have serial numbers starting with 28159-28160.
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 BA X-ray machines because a power supply issue may cause the X-ray tube to stop working during procedures. This could lead to incomplete imaging and potential delays in medical care.
The power supply in the generator control can fail sporadically above a specific voltage threshold. When this happens during an X-ray procedure, the X-ray tube stops receiving required voltage, making X-rays impossible. This risk occurs during ongoing procedures, potentially causing incomplete imaging.
Healthcare facilities using the specific model and serial numbers listed are most at risk. Patients undergoing X-ray procedures with these machines may experience interrupted imaging.
Check if your machine has the model number 5904656 and serial numbers starting with 28159, 28144, 28154, 28139, 28155, or 28160. These units were sold with specific serial numbers listed in the recall notice.
Verify your AXIOM Artis BA machine's model number and serial numbers against the list provided in the recall notice.
The power supply in the generator control may fail sporadically above a specific voltage threshold, causing the X-ray tube to stop working during procedures.
Check your machine's model number and serial numbers against the list provided in the recall notice. Siemens has not yet specified a remedy for this issue.
Yes, the issue can cause X-ray tube failure during procedures, potentially leading to incomplete imaging and delays in medical care.
We’ve drafted a message you can send Siemens Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2016-2019 — Siemens Medical Siemens Medical Hello, I own a Siemens Medical that is covered by recall Z-2016-2019 from Siemens Medical. 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.
