Siemens recalls Artis zee floor Interventional Fluoroscopic X-Ray Systems with model 10094142 and software VC21C due to collision sensor causing tabletop movement delays during procedures.
In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor will cause a block the movement of the floating tabletop and could result in a delay or interruption of a procedure.
Siemens is recalling Artis zee floor Interventional Fluoroscopic X-Ray Systems with specific model and software versions. The recall is because a collision sensor might block tabletop movement, potentially delaying medical procedures.
The collision sensor in the affected systems may block the tabletop's movement during procedures. This could cause delays or interruptions in medical treatments that require continuous imaging.
Healthcare facilities using the affected Artis zee systems are most at risk. Patients undergoing procedures with these systems could experience delays.
Check for model number 10094142 and software version VC21C. Affected units have serial numbers 140422, 140423, or 140430.
Verify your Artis zee system's model number, software version, and serial number to confirm if it's affected.
Model number 10094142 with software version VC21C.
Serial numbers 140422, 140423, and 140430.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0695-2020 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0695-2020 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.
