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Recall Observatory FDA recall evidence

Device product

SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

Z-1239-2026

December 19, 2025

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 98206
Status
Ongoing
Classification
Class II
Quantity
2 units
Official record key
device-enforcement:Z-1239-2026

Official wording

Reason: To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.

Code information: Material Number: 11330002; UDI-DI: 04056869231051; Serial Numbers: 125205, 125250;

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Canada, Costa Rica, India, Israel.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.