Siemens recalls Artis Q angiography systems with serial numbers 105121-105125, 111127-111130, 123239-123246. The floating tabletop may become blocked after a collision sensor triggers during system movement, potentially causing system malfunctions.
In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.
Siemens is recalling Artis Q angiography systems with specific serial numbers because the floating tabletop can become blocked after a collision sensor activates during system movement. This could lead to system malfunctions during medical procedures.
The collision sensor in the system may activate during movement, causing the floating tabletop to become blocked. This blockage could lead to system malfunctions during medical procedures, potentially affecting patient safety.
Medical professionals using Siemens Artis Q systems with the listed serial numbers are most at risk. These systems are used for diagnostic imaging and interventional procedures in hospitals and clinics.
Check the serial number on your Artis Q system. Affected units have serial numbers 105121-105125, 111127-111130, or 123239-123246.
Identify your Artis Q system's serial number to determine if it is affected by this recall.
The floating tabletop may become blocked after a collision sensor activates during system movement, which could cause system malfunctions during medical procedures.
Systems with serial numbers 105121-105125, 111127-111130, or 123239-123246 are affected.
The recall does not specify a remedy, so contact Siemens directly for guidance on next steps.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1342-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1342-2019 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.
