Siemens recalls specific AXIOM Artis dBA X-ray machines (model 7555357) due to power supply tolerance issues that can prevent X-ray function during procedures.
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 dBA 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 has a tolerance issue that can cause generator A100 failure when power exceeds a specific threshold. This prevents the X-ray tube from receiving required voltage, making X-ray imaging impossible during procedures. The issue occurs sporadically but may happen mid-procedure.
Healthcare facilities using the specific model and serial numbers listed in the recall. Patients undergoing X-ray procedures with these machines are at risk of incomplete imaging.
Check if your X-ray machine has the model number 7555357 and one of the listed serial numbers (e.g., 53181, 53023, 53167). The recall applies to machines sold with these identifiers.
Verify your X-ray machine's model number and serial numbers against the list provided in the recall notice.
A power supply tolerance issue can cause generator A100 failure, preventing the X-ray tube from receiving required voltage during procedures.
Check if your machine has model number 7555357 and one of the listed serial numbers (e.g., 53181, 53023, 53167).
The recall does not specify a remedy, so contact Siemens directly for guidance on next steps.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2022-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2022-2019 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.
