Siemens recalls Artis zee floor model 10094135 for angiography and fluoroscopy procedures due to display issues that may cause treatment interruptions if the screen goes black without error messages.
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 its Artis zee floor model 10094135 for angiography and fluoroscopy procedures because the large display may go black without showing an error message after power save mode, potentially requiring treatment cancellation or system restart. This could disrupt medical procedures if the display fails during X-ray imaging.
After the large display returns from power save mode, it may go black without showing an error message while X-ray is still possible. This can cause the system to become unresponsive, requiring treatment cancellation or system restart. The problem does not occur during ongoing procedures.
Medical facilities using Siemens Artis zee floor model 10094135 for X-ray procedures are most at risk. Patients undergoing angiography or fluoroscopy may experience treatment interruptions if the display fails.
Check for the model number 10094135 on the Artis zee floor system used for angiography and fluoroscopy procedures. This recall applies to systems sold in the U.S. between specific dates.
Ensure the large display shows images after returning from power save mode without blacking out.
No, this recall specifically applies to model 10094135 for angiography and fluoroscopy procedures.
The system may need to be restarted or treatment canceled; contact Siemens for further instructions.
The recall record does not specify a fix or remedy.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2311-2018 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2311-2018 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.
