PlainRecalls
FDA Devices Moderate Class II Terminated

Syngo.Via VB20A model 1049610

Reported: May 16, 2018 Initiated: March 27, 2018 #Z-1778-2018

Product Description

Syngo.Via VB20A model 1049610

Reason for Recall

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.

Details

Units Affected
N/A
Distribution
Nationwide
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
Syngo.Via VB20A model 1049610. Recalled by Siemens Medical Solutions USA, Inc. Units affected: N/A.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 16, 2018. Severity: Moderate. Recall number: Z-1778-2018.