Siemens Medical Solutions USA, Inc recalls Syngo.Via VB20A model 1049610

Recall date

March 27, 2018

Source

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

Recall number

Z-1778-2018

FDA classification

Class II

Brand / firm

Siemens Medical Solutions USA, Inc

Sold / distributed

Nationwide

Why it was recalled

Functionality in the report sections "Findings Information" and "Summary of Measured Findings" not functioning properly. The corrected values modified in the report are neither saved, nor printed, nor sent to the information system. The system will still use original values.

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 VB20A model 1049610