Siemens recalls Artis Q.zeego models with material no. 10848283 for potential black screen after power save, affecting angiography and fluoroscopy procedures. No immediate safety risk but may disrupt imaging.
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 Q.zeego medical imaging systems with material number 10848283 because the large display may stay black without error messages after returning from power save mode. This could require canceling procedures or switching to another system, but it does not cause injury during normal use.
After the large display returns from power save mode, it may show a black screen without an error message while X-ray imaging is still possible. This can cause the system to become unresponsive, potentially requiring procedure cancellation or patient transfer to another system.
Medical professionals using Siemens Artis Q.zeego systems for angiography or fluoroscopy procedures. Patients may be affected if procedures are interrupted.
Check for the material number 10848283 on the Artis Q.zeego system. The product was sold in the U.S. between 2018 and 2020, with specific model numbers listed in the recall notice.
Ensure the large display shows an image after returning from power save mode; if it stays black without error messages, the system may be affected.
No, the recall does not involve injury risk. The issue only affects system functionality during imaging procedures.
Check for the material number 10848283 on the system. The product was sold in the U.S. between 2018 and 2020.
The system may need to be canceled or transferred to another system; contact Siemens for further instructions.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2306-2018 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2306-2018 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.
