Siemens recalls Artis Q.zen biplane angiography systems with software VD12- that may cause procedure delays if x-ray is not released during SID lift movement. Affected units have specific model and serial numbers.
If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result in a short delay in procedure
Siemens is recalling Artis Q.z:en biplane angiography systems with software version VD12- due to a potential delay in x-ray procedures if the source-to-image distance lift movement is activated. This could cause a short delay in medical procedures but does not pose a safety risk to patients or users.
When the source-to-image distance (SID) lift movement is activated and x-ray release happens at the same time, the system may display 'No x-ray, try again' instead of proceeding with the x-ray. This causes a short delay in the procedure but does not cause injury or damage.
Medical facilities using Siemens Artis Q.zen biplane systems with software VD12- are affected. Staff operating these systems may experience brief delays during procedures.
Check for model number 10848355 or serial numbers 123502 and 123501 on the system. These units were sold with software version VD12- for diagnostic imaging and interventional procedures.
Identify the model number (10848355) and serial numbers (123502, 123501) on your Artis Q.zen biplane system.
No, the recall does not pose a safety risk. The issue causes only a short delay in procedures, not injury or damage.
Check the model number and serial numbers to confirm if your system is affected. The recall does not require immediate action beyond verification.
Affected systems have model number 10848355 and serial numbers 123502 or 123501. These units were sold with software version VD12- for diagnostic imaging.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0305-2022 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0305-2022 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.
