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Siemens Medical Solutions USA, Inc recalls Syngo.via systems with SW VB20A
Recalled March 7, 2018 · FDA recall Z-0808-2018 · Siemens Medical Solutions USA
Hazard
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. · FDA Class II
Units
30
Sold at
Nationwide Distribution.
Description
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.
Product
Syngo.via systems with SW VB20A
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →