Olympus Corporation of the Americas: Medical Device Recall in 2023 - (Recall #: Z-2467-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V

Product Classification:

Class II

Date Initiated: July 27, 2023

Date Posted: September 6, 2023

Recall Number: Z-2467-2023

Event ID: 92703

Reason for Recall:

Recent reports of patient infection.

Status: Ongoing

Product Quantity: 6,426 units

Code Information:

Model No. TJF-Q190V; UDI-DI: 04953170405563; All Serial No.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated