Siemens recalls Artis zee floor MN model 10094142 due to power supply issues causing X-ray tube failure during procedures. Affected units have specific serial numbers listed in the recall notice.
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 MN model 10094142 because a power supply tolerance issue may cause the X-ray tube to stop working during procedures. This could prevent X-ray imaging from being possible while a patient is being scanned.
The power supply in the generator control has a tolerance issue that can cause generator A100 failure when the voltage exceeds a specific threshold. This may lead to the X-ray tube not receiving required voltage, making X-ray imaging impossible during an ongoing procedure.
Medical facilities using the Artis zee floor MN model 10094142 with specific serial numbers are affected. Patients undergoing X-ray procedures with this equipment may be at risk if the issue occurs during their scan.
Check if your Artis zee floor MN has model number 10094142 and one of the listed serial numbers: 140212, 140115, 140101, 140205, 140213, 140204, 140209, 140219, 140224, 140218, 140221, 140220, 140206, 140223, 140105, 140226, 140108, 140102, 140109, 140100, 140202, 140214, 140114.
Verify your Artis zee floor MN has model number 10094142 and one of the listed serial numbers.
The power supply in the generator control has a tolerance issue that may cause generator A100 failure during procedures, preventing the X-ray tube from receiving required voltage.
The recall notice does not specify a remedy or action for affected units. Check the model and serial numbers to confirm if your unit is affected.
The recall states the issue may occur during an ongoing procedure, but the notice does not describe specific injury risks or mechanisms.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2032-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2032-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
