Siemens recalls ARTIS icono ceiling model 11328100 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 ceiling model 11328100 because adjusting the detector lift height to maximum or minimum limits can cause loss of movement capability. This means the device might not function properly after extreme adjustments, potentially affecting medical imaging procedures.
The device can lose movement capability when the detector lift height is adjusted to its maximum or minimum limits. This could cause the imaging equipment to malfunction during medical procedures, potentially affecting the accuracy or safety of the imaging process.
Medical facilities using the ARTIS icono ceiling model 11328100 are most at risk, particularly those with specific serial numbers listed in the recall. Patients using this equipment for imaging may be affected if the device malfunctions.
Check if your ARTIS icono ceiling has model number 11328100 and one of the listed serial numbers (e.g., 194180, 194184, 194169). The recall includes specific serial numbers provided in the official notice.
Verify your ARTIS icono ceiling has model number 11328100 and one of the listed serial numbers (e.g., 194180, 194184, 194169).
Adjusting the detector lift height to maximum or minimum limits can cause loss of movement capability in the ARTIS icono ceiling.
Check if your ARTIS icono ceiling has model number 11328100 and one of the specific serial numbers listed in the recall notice.
The recall does not specify a remedy, so no action is required beyond checking if your unit is affected.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2642-2026 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2642-2026 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.
