Siemens recalls Artis zee and Artis Q imaging systems due to potential collision with room equipment causing patient or staff injury. Affected models include Artis Q Biplane, Ceiling, Floor, and ZeeGO systems with specific serial numbers.
Potential exists for the collision supervision not to work properly following loss of the individual room configuration data settings causing danger of collision with fix mounted room equipment, walls or floor may occur. This might cause components of the system to fall or tilt which could result in crushing of patients, operators or staff, collision of system parts with patients, as well as result in delay or interruption of the clinical procedure
Siemens is recalling Artis zee and Artis Q imaging systems because a software issue might cause the system to collide with fixed equipment, risking injury to patients or staff. This could lead to equipment falling or tilting during procedures.
If the room configuration data settings are lost, the collision supervision system may fail. This could cause the imaging system to move into fixed equipment, walls, or floors, potentially crushing patients or staff and interrupting procedures.
Healthcare facilities using Artis zee or Artis Q systems for medical imaging are affected. Staff and patients at facilities with the recalled models are at risk during procedures.
Check for Artis Q or Artis zee systems with specific model numbers listed in the recall (e.g., Artis Q Biplane, Ceiling, Floor). The serial numbers provided in the recall list indicate affected units.
Identify your system model from the list of Artis Q or Artis zee systems provided in the recall notice.
Confirm your system's serial number matches the list of affected numbers provided in the recall.
Artis Q Biplane, Ceiling, Floor, ZeeGO, and Artis zee Biplane, Ceiling, Floor, and Multi-purpose systems with specific serial numbers listed in the recall.
The recall notice does not specify a remedy; affected units must be checked against the provided serial numbers.
Check your system model against the list of Artis Q or Artis zee models and verify your serial number against the provided list of affected numbers.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0108-2021 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0108-2021 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.