Olympus Corporation of the Americas: Medical Device Recall in 2019 - (Recall #: Z-1008-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.

Product Classification:

Class II

Date Initiated: December 17, 2018

Date Posted: March 20, 2019

Recall Number: Z-1008-2019

Event ID: 82099

Reason for Recall:

The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.

Status: Terminated

Product Quantity: 1

Code Information:

Serial Number 2418319

Distribution Pattern:

US Nationwide distribution in the states of CT, IL, MN, MO, and NC.

Voluntary or Mandated:

Voluntary: Firm initiated