# FDA recall Z-2706-2017

> **Fujifilm Medical Systems U.S.A., Inc.** · Class II · device recall initiated 2017-02-17.

## Product

Ultrasonic Endoscope  Model Number EG-530UT    A flexible ultrasonic endoscope intended to provide ultrasonic images of submucosal and peripheral organs

## Reason for recall

Fujifilm is recalling multiple endoscopes after a retrospective review.

## Distribution

US Distribution to : AL, HI and MO

## Key facts

- **Recall number:** Z-2706-2017
- **Recalling firm:** Fujifilm Medical Systems U.S.A., Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-02-17
- **Report date:** 2017-07-19
- **Termination date:** 2018-10-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wayne, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2706-2017

## Citation

> AI Analytics. FDA recall Z-2706-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2706-2017. Source: US FDA. Licensed CC0.

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