# FDA recall Z-1778-2018

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2018-03-27.

## Product

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

Nationwide

## Key facts

- **Recall number:** Z-1778-2018
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-27
- **Report date:** 2018-05-16
- **Termination date:** 2020-06-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Malvern, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1778-2018

## Citation

> AI Analytics. FDA recall Z-1778-2018. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1778-2018. Source: US FDA. Licensed CC0.

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