# FDA recall Z-2709-2017

> **Toshiba American Medical Systems Inc** · Class II · device recall initiated 2017-05-01.

## Product

XARIO 200 TUS-X200  diagnostic ultrasound system

## Reason for recall

When Continuous Trace method is used as the tracing method on Spectral Doppler in velocity trace measurement, an incorrect value may be displayed in the ultrasound systems and in the ultrasound workstations listed below.

## Distribution

Nationwide Distribution

## Key facts

- **Recall number:** Z-2709-2017
- **Recalling firm:** Toshiba American Medical Systems Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-01
- **Report date:** 2017-07-19
- **Termination date:** 2023-10-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tustin, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2709-2017

## Citation

> AI Analytics. FDA recall Z-2709-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2709-2017. Source: US FDA. Licensed CC0.

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