# FDA recall Z-1920-2019

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2019-06-04.

## Product

SOMATOM go.Now, Model No. 11061618    with syngo.CT software versions VA20A,  VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. This CT system can be used for low dose lung cancer screening in high risk populations. High risk populations are as defined by professional medical societies.

## Reason for recall

The potential sporadic performance problems  may cause scanning workflow interruptions and  unexpected user notifications resulting in  diagnostic delay or need for patient rescan.

## Distribution

US Nationwide distribution in the states of AL  CA  CT  FL  GA  IL  IN  KS  KY  LA  ME  MI  MO  MS  NC  ND  NE  NH  NY  OH  OK  SD  TN  TX  VA and   WI

## Key facts

- **Recall number:** Z-1920-2019
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-04
- **Report date:** 2019-07-10
- **Termination date:** 2023-03-29

- **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-1920-2019

## Citation

> AI Analytics. FDA recall Z-1920-2019. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/Z-1920-2019. Source: US FDA. Licensed CC0.

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