Siemens recalls Artis zee floor Model 10094135 with serial numbers listed. A power supply tolerance issue may cause X-ray tube failure during procedures, preventing X-ray imaging. Affected units must be checked for serial numbers.
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 Artis zee floor models with specific serial numbers due to a power supply issue that can cause X-ray tube failure during procedures. This means the machine may not produce X-rays when needed, potentially disrupting medical imaging.
The power supply has a tolerance issue that can cause generator A100 failure when power exceeds a specific value. This prevents the X-ray tube from receiving required voltage, making X-ray imaging impossible during procedures. The issue occurs sporadically but may happen during an ongoing procedure.
Medical facilities using the Artis zee floor model with serial numbers listed in the recall. Patients undergoing X-ray procedures may be affected if the machine fails during their treatment.
Check the serial number on the Artis zee floor model. The affected units have specific serial numbers listed in the recall notice (e.g., 135944, 135746, etc.).
Look for the serial number on the Artis zee floor model to confirm if it is affected.
A tolerance issue in the power supply may cause generator A100 failure, preventing X-ray tube operation during procedures.
Check the serial number against the list provided in the recall notice to see if your unit is affected.
The recall record does not specify a remedy, so no fix is currently available.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2028-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2028-2019 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.
