Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 Recalled by Siemens Medical Solutions USA, Inc Due to software syngo.CT VB20 in the installed base, with...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Medical Solutions USA, Inc directly.
Affected Products
SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000
Quantity: 64 units
Why Was This Recalled?
software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in the delay in diagnosis, the necessity for patient rescans, and/or the need for additional contrast media may occur
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Siemens Medical Solutions USA, Inc
Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report