Olympus Corporation of the Americas: Medical Device Recall in 2022 - (Recall #: Z-1116-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Olympus Uretero-reno videoscope, Model No. URF-V2

Product Classification:

Class II

Date Initiated: March 25, 2022

Date Posted: May 25, 2022

Recall Number: Z-1116-2022

Event ID: 90063

Reason for Recall:

The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.

Status: Ongoing

Product Quantity: 1

Code Information:

1 unit, serial number 2825505F UDI 04953170343582

Distribution Pattern:

US Nationwide distribution in the state of AZ.

Voluntary or Mandated:

Voluntary: Firm initiated