Siemens recalls Artis Q angiography systems with serial numbers 103277-121506 due to risk of floating tabletop getting stuck after collision sensor activation during use. Affected units may require repair to prevent potential 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 if not addressed.
The collision sensor in affected Artis systems may activate during movement, causing the floating tabletop to become blocked. This blockage could lead to system malfunctions during procedures, potentially affecting patient safety and procedure outcomes.
Medical professionals using Siemens Artis Q angiography systems for procedures like cardiac or neuro angiography are most at risk. Patients undergoing imaging with these systems may also be affected if the equipment malfunctions.
Check for Artis Q angiography systems with serial numbers listed in the recall (103277 to 121506). The product is used for medical imaging procedures including cardiac and neuro angiography.
Identify your Artis Q system's serial number to confirm if it is in the recall list (103277-121506).
If your system is affected, contact Siemens Medical Solutions USA, Inc for repair assistance as the remedy is not specified in the recall record.
The floating tabletop may become blocked after a collision sensor activates during system movement, potentially causing system malfunctions.
Serial numbers 103277 through 121506 (as listed in the recall).
No, the recall does not require immediate stop use; however, affected systems should be repaired to prevent potential malfunctions.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1341-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1341-2019 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.
