Siemens recalls Artis Icono X-Ray System model 11327600 due to potential electrical failure from increased fan wear during system tests, which could cause image system malfunction.
During system tests, an increased wearing of the Image acquisition system fans has been observed. This could lead to an electrical failure which may cause malfunction of the image system during regular system operation.
Siemens is recalling its Artis Icono Interventional Fluoroscopic X-Ray System (model 11327600) because tests show increased wear on image acquisition system fans. This could lead to electrical failures that might cause the image system to malfunction during regular use.
The image acquisition system fans are wearing out faster than expected during tests. This increased wear could cause electrical failures, which might lead to the image system malfunctioning during regular medical procedures.
Medical facilities using the Artis Icono X-Ray System with model number 11327600 are affected. Staff and patients using this system during procedures may be at risk if the image system malfunctions.
Check for the model number 11327600 on the Artis Icono X-Ray System. The serial numbers listed in the recall include 180062, 180054, and other numbers starting with 1800.
Identify the model number on your Artis Icono X-Ray System; the recalled model is 11327600.
The recall indicates potential electrical failure from increased fan wear, which could cause image system malfunction during use. However, the hazard is not described as causing serious injury or death in normal use.
Check for the model number 11327600 on your Artis Icono X-Ray System. The serial numbers listed in the recall include specific numbers starting with 1800.
The recall does not specify a remedy, so affected users should contact Siemens directly 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-1342-2022 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1342-2022 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.
