Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Syngo.via systems with SW VB20A Recalled by Siemens Medical Solutions USA, Inc Due to A software update was released on August 22,...
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
Syngo.via systems with SW VB20A
Quantity: 30
Why Was This Recalled?
A software update was released on August 22, 2017. Performing this software installation and upgrading syngo.via system to the software version VB20A_HF02 will resolve various bugs and inconsistent diagnosis with the old system.
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