Siemens recalls Artis zee ceiling models with material no. 10094137 for angiography procedures due to potential display failure after power save mode, requiring treatment cancellation or system restart.
After the Large Display returns from power save mode, it may not show an image, and stay black without showing an error message although X-ray is still possible. The problem does not occur during an ongoing procedure. If the problem occurs, the system cannot be operated normally. It may be necessary to cancel or restart the treatment or transfer the patient to an alternate or another system.
Siemens is recalling Artis zee ceiling systems with material number 10094137 for angiography and fluoroscopy procedures. The display may go black without showing an error message after returning from power save mode, which could prevent the system from operating normally during procedures and require treatment cancellation or transfer to another system.
After the display returns from power save mode, it may show black screen without an error message while X-ray is still possible. This causes the system to become unresponsive, potentially requiring treatment cancellation or patient transfer to another system during procedures.
Medical professionals using Siemens Artis zee ceiling systems for angiography and fluoroscopy procedures with material number 10094137 are most at risk. This affects patients undergoing these procedures when the system malfunctions.
Check for the material number 10094137 on the Artis zee ceiling system used for angiography and fluoroscopy procedures. This model was sold for specific medical imaging applications.
After returning from power save mode, the display may show black screen without error message while X-ray is still possible.
If the display goes black without showing an error message, stop the procedure and transfer the patient to another system.
No, this recall specifically affects Artis zee ceiling systems with material number 10094137 used for angiography and fluoroscopy procedures.
If the display goes black without showing an error message, stop the procedure and transfer the patient to another system.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2310-2018 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2310-2018 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.
