Siemens SOMATOM Definition Flash CT Scanners May Cause Scan Abort - Recall

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Recalling firmSiemens Medical Solutions USA, Inc40 Liberty Blvd, N/A · Malvern, PA 19355-1418

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Siemens is recalling certain SOMATOM Definition Flash CT scanners that may cause scans to abort due to software issues. This could delay or interrupt medical imaging procedures for patients.

Why it’s dangerous

The software issues in syngo.CT version VB10A could cause the CT scanner to stop a scan prematurely. This might lead to incomplete imaging, requiring additional scans or re-evaluation.

Who’s affected

Patients and medical staff using the recalled CT scanners may experience delayed imaging procedures. The risk is low as the issue only affects scan completion, not patient safety during the scan.

How to tell if you have this one

Check for model number 10430603 on the scanner. Affected units have serial numbers starting with 73008 or 98642.

Brand
Siemens
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Scanner Model
Identify the model number on your scanner; affected units are model 10430603.
Verify Serial Number
Check if your scanner's serial number starts with 73008 or 98642.

✎ GovInfoNow

Questions people ask

What is the model number of the recalled CT scanners?

The recalled model number is 10430603.

What serial numbers are affected?

Serial numbers starting with 73008 or 98642 are affected.

Why is this recall happening?

The recall is due to potential software issues that may cause scan aborts in syngo.CT version VB10A.

Take action

Contact Siemens

We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2270-2019 — Siemens Siemens

Hello,

I own a Siemens that is covered by recall Z-2270-2019 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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Where this comes from

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.

Official source: FDA Recall #Z-2270-2019 (July 3, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2270-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Siemens Medical Solutions USA, Inc recalls SOMATOM Definition Flash, Model Number 10430603 - Product Usage: Computed tomography systems intended to generate and

Lower-risk recall