FDA Medical devices recall ·
SOMATOM X.ceed Software applications: syngo.CT Brain Quantification… recall
- Recall number
- Z-1239-2026
- Date
- (initiated December 19, 2025)
- Company / brand
- Siemens Medical Solutions USA, Inc
40 Liberty Blvd, Malvern, PA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 2 units
- Hazard tags
- Software
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS
Why was it recalled?
To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Material Number: 11330002; UDI-DI: 04056869231051; Serial Numbers: 125205, 125250;
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Costa Rica, India, Israel.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1239-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.