Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Ultrasonic Endoscope Model Number EG-530UT A flexible ultrasonic endoscope intended Recalled by Fujifilm Medical Systems U.S.A., Inc. Due to Fujifilm is recalling multiple endoscopes after a retrospective...

Date: February 17, 2017
Company: Fujifilm Medical Systems U.S.A., Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Fujifilm Medical Systems U.S.A., Inc. directly.

Affected Products

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

Quantity: 4 units

Why Was This Recalled?

Fujifilm is recalling multiple endoscopes after a retrospective review.

Where Was This Sold?

This product was distributed to 3 states: AL, HI, MO

Affected (3 states)Not affected

About Fujifilm Medical Systems U.S.A., Inc.

Fujifilm Medical Systems U.S.A., Inc. has 37 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report