Siemens recalls SOMATOM Spirit CT scanners with serial numbers 31621, 31245, : potential unnecessary radiation exposure due to software issue. Affected units may need repair or software update.
A potential risk of unnecessary radiation exposure due to a software issue
Siemens is recalling specific models of SOMATOM Spirit CT scanners because a software issue could cause unnecessary radiation exposure. This means some scans might be less safe than intended, potentially increasing health risks for patients and staff.
A software issue in the scanner could cause it to emit radiation without proper safety checks. This might lead to unnecessary radiation exposure during scans, though the risk is not severe enough to cause immediate harm.
Patients and medical staff using the recalled SOMATOM Spirit CT scanners with specific serial numbers are most at risk. The recall affects only the listed units, not all Siemens CT scanners.
Check if your scanner has the model number 10045692 and the listed serial numbers: 31621, 31245, 79670, 31092, 31313, 31611. The recall applies only to these specific units.
Identify your scanner's model number and serial numbers to confirm if it is affected by this recall.
The recall is due to a software issue that could cause unnecessary radiation exposure during scans.
No, the recall does not require immediate stop use. Affected units may need software updates or repairs.
Check for the model number 10045692 and the specific serial numbers listed: 31621, 31245, 79670, 31092, 31313, 31611.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2478-2018 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2478-2018 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.
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.