Siemens recalls Artis Pheno Interventional Fluoroscopy Systems with model 10849000 due to rare video signal loss in displays, potentially causing image loss during procedures. Affected units include specific serial numbers listed in the recall.
A video signal from one of the transceivers of the Large Display may be lost. In very rare cases, both transceivers of the Large Display could potentially fail which can lead to the loss of both video signals. This issue can sporadically affect the Large Display in the examination room as well as the displays in the control room.
Siemens is recalling Artis Pheno X-ray systems with model number 10849000 because a video signal from the Large Display could be lost, which might cause image loss during medical procedures. This issue is rare but could affect both the examination room and control room displays.
The system's Large Display may lose video signals from one or both transceivers, causing image loss during medical procedures. This issue is rare but could affect both the examination room and control room displays.
Healthcare facilities using the Artis Pheno system with model 10849000 are affected. Medical staff and patients using the system during procedures may be at risk if the display fails.
Check for the model number 10849000 on the system. Affected units have specific serial numbers listed in the recall notice, including many numbers starting with 164000.
Review the serial numbers listed in the recall notice to confirm if your system is affected.
The recall states this issue is rare and could cause image loss during procedures, but it does not mention serious injury risk.
Check for the model number 10849000 and the specific serial numbers listed in the recall notice.
The recall does not require stopping use; it only lists affected units for verification.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1294-2022 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1294-2022 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.
