Siemens recalls two models of SOMATOM go.Top CT scanners due to missing dose documentation and dose alert features during interventional procedures, which could lead to radiation exposure risks.
SOMATOM go.Top (Models #11061640 & 11061648) with software syngo CT VA20A_SP2 and active Guide&GO license No dose documentation and no Dose Alert for the special mode i- Sequence during interventional procedures
Siemens is recalling two specific models of SOMATOM go.Top CT scanners because they lack dose documentation and dose alerts during certain medical procedures. This could result in unintended radiation exposure for patients during interventional procedures.
The recalled CT scanners do not have dose documentation or dose alerts for special modes used during interventional procedures. This means radiation exposure levels could be higher than intended without proper monitoring.
Healthcare facilities using the recalled models of Siemens SOMATOM go.Top CT scanners are most at risk. Patients undergoing interventional procedures with these scanners may face radiation exposure risks.
Check for the model numbers 11061640 or 11061648 on the scanner's label. These are specific Siemens SOMATOM go.Top CT scanners with software syngo CT VA20A_SP2 and active Guide&GO license.
Identify the model number on the scanner's label to confirm if it is 11061640 or 11061648.
The recall is due to the absence of dose documentation and dose alerts for special modes during interventional procedures, which could lead to unintended radiation exposure.
The official recall notice does not specify a remedy or action steps for affected scanners.
The recall indicates a potential risk of unintended radiation exposure during interventional procedures, but the official notice does not specify serious injury risks.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0265-2020 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0265-2020 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.
