Siemens Medical recalls SOMATOM Emotion 6 CT scanners (Model 10165888) due to a software issue that may cause unnecessary radiation exposure during scans.
A potential risk of unnecessary radiation exposure due to a software issue
Siemens is recalling its SOMATOM Emotion 6 CT scanners (Model 10165888) because a software issue could lead to unnecessary radiation exposure during medical scans. This affects patients and healthcare providers who use the device, as radiation exposure can pose health risks.
The software issue in the SOMATOM Emotion 6 CT scanner may cause it to emit radiation during scans without proper safety checks. This could lead to unnecessary radiation exposure for patients and staff during medical imaging procedures.
Patients and healthcare providers using the SOMATOM Emotion 6 CT scanner (Model 10165888) are affected. Medical facilities that have this model are most at risk of unnecessary radiation exposure.
Check for the model number 10165888 on the scanner's label. The recall applies to this specific model of Siemens SOMATOM Emotion 6 CT scanner.
Identify the model number on your scanner's label to confirm if it is the recalled SOMATOM Emotion 6 (Model 10165888).
The recall is for a potential risk of unnecessary radiation exposure, but the risk level is low. Siemens states this is not an immediate hazard but requires attention.
Check for the model number 10165888 on the scanner's label. This specific model is affected by the recall.
The recall does not specify a remedy, so contact Siemens Medical Solutions for further guidance on potential actions.
We’ve drafted a message you can send Siemens Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2472-2018 — Siemens Medical Siemens Medical Hello, I own a Siemens Medical that is covered by recall Z-2472-2018 from Siemens Medical. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.