Siemens recalls ARTIS Icono Biplane model 11327600 due to potential loss of movement capability when adjusting detector lift height to max or min limits. Affected units have specific serial numbers.
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Siemens is recalling its ARTIS Icono Biplane medical imaging device with model number 11327600. Adjusting the detector lift height to maximum or minimum limits could cause loss of movement capability, which may impact medical procedures.
The device's detector lift height adjustment can become unstable when set to maximum or minimum limits. This instability may lead to loss of movement capability, potentially affecting the accuracy or safety of medical imaging procedures.
Medical facilities using the ARTIS Icono Biplane model 11327600 are affected. Patients undergoing imaging procedures with this device may be at risk if the detector height adjustment causes movement issues.
Check for model number 11327600 on the device. Affected units have specific serial numbers listed in the recall notice, including 184246, 184241, and other serial numbers provided in the recall.
Verify the model number is 11327600 on the ARTIS Icono Biplane device.
Reach out to Siemens Medical Solutions USA, Inc for further assistance with the recall.
The recalled model number is 11327600 for the ARTIS Icono Biplane.
Check if your ARTIS Icono Biplane has model number 11327600 and one of the listed serial numbers, such as 184246 or 184241.
Contact Siemens Medical Solutions USA, Inc for guidance on next steps, as the recall does not specify a specific action beyond checking the model and serial numbers.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2641-2026 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2641-2026 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.
