Siemens Medical Solutions USA, Inc recalls Syngo.via systems with SW VB20A

Recall date

August 31, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0808-2018

FDA classification

Class II

Brand / firm

Siemens Medical Solutions USA, Inc

Sold / distributed

Nationwide Distribution.

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Syngo.via systems with SW VB20A