NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS
FDA Recall Z-1240-2026 · Posted 2026-02-03
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Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusOpen, Classified
Product CodeJAK
Date Initiated2025-12-19
Product Quantity88 units
Reason for Recall
To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.
Firm Action
On December 19, 2025, CUSTOMER ADVISORY NOTICE letters were sent to customers.
Actions to be taken:
1. Stop all use of the Applications in patient care setting.
2. Please notify and instruct all staff at your organization who need to be aware of this matter.
3. Please ensure that all users of the affected products within your organization and others who may need to be informed will receive the relevant safety information provided within this notice and will comply with the recommendations therein.
4. Please ensure that this advisory notice is retained in your product related records appropriately. Please keep this information until the corrective measures have been finalized.
Actions by Siemens:
Siemens Healthineers is expeditiously working to remove the Applications from your CT system(s) through a software update process. Our service organization will contact you shortly to arrange a date to perform this corrective action.
Please feel free to contact our service organization at 1-800-888-7436 if you have any questions.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Canada, Costa Rica, India, Israel.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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