Home / Recalls / Siemens Medical Solutions USA, Inc / Z-1778-2018

Z-1778-2018 Class II Terminated

Recalled by Siemens Medical Solutions USA, Inc — Malvern, PA

FDA device recall Z-1778-2018 was initiated by Siemens Medical Solutions USA, Inc on Mar 27, 2018 and is designated Class II. 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… The recall status is terminated (terminated Jun 15, 2020).

Recall Details

Product Type: Devices
Report Date: May 16, 2018
Initiation Date: Mar 27, 2018
Termination Date: Jun 15, 2020
Voluntary/Mandated: Voluntary: Firm initiated

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.

Distribution Pattern

Nationwide

Code Information

All

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-1778-2018
openFDA file date: Oct 26, 2026
Loaded by RegDataLab: Oct 27, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.