Siemens recalls SOMATOM Scope CT scanners with serial numbers starting 90811 to 99305 due to potential unnecessary radiation exposure from a software issue. Affected units may require software updates to reduce radiation risk.
A potential risk of unnecessary radiation exposure due to a software issue
Siemens is recalling certain SOMATOM Scope CT scanners because a software issue could lead to unnecessary radiation exposure during medical imaging. This means patients and staff might receive higher radiation doses than intended, which could pose health risks over time.
The software issue causes the scanner to sometimes deliver radiation doses higher than necessary for medical imaging. This could lead to unnecessary radiation exposure for patients and medical personnel during scans, though the risk is not immediate or severe.
Medical facilities using the recalled SOMATOM Scope CT scanners with specific serial numbers are most at risk. Patients and staff during scans may be exposed to higher radiation levels than intended.
Check if your SOMATOM Scope CT scanner has a serial number starting with 90811 and ending with 99305 (e.g., 90811, 91203, 99305). The model number is 10967666.
Verify your scanner's serial number starts with 90811 and ends with 99305 (e.g., 90811, 91203, 99305).
Siemens identified a software issue that could cause unnecessary radiation exposure during medical imaging, so they are recalling affected units.
No, the recall does not require immediate stoppage. Affected units may need software updates to reduce radiation risk.
Check the serial number on your scanner; affected units have serial numbers starting with 90811 and ending with 99305 (e.g., 90811, 91203, 99305).
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2476-2018 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2476-2018 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.
