Fujifilm Medical Systems U.S.A., Inc.: Medical Device Recall in 2017 - (Recall #: Z-2706-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: February 17, 2017

Date Posted: July 19, 2017

Recall Number: Z-2706-2017

Event ID: 76899

Reason for Recall:

Fujifilm is recalling multiple endoscopes after a retrospective review.

Status: Terminated

Product Quantity: 4 units

Code Information:

1U881A131 1U88A1A145 3U881A005

Distribution Pattern:

US Distribution to : AL, HI and MO

Voluntary or Mandated:

Voluntary: Firm initiated