Olympus Corporation of the Americas: Medical Device Recall in 2022 - (Recall #: Z-1274-2022)

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:

Colonovideoscope Model CF-H180AL

Product Classification:

Class II

Date Initiated: April 22, 2022

Date Posted: June 29, 2022

Recall Number: Z-1274-2022

Event ID: 90218

Reason for Recall:

A (Camera unit) CCD intended for a different model of colonoscope may have been installed in the CF-H180AL, viewing angle would be narrower than a normal CF-H180AL and the use of EndoTherapy devices may stick out (approximately 1.4 mm) further than normal protrusion,could lead to patient injury; specifically, mucosal damage that could result in hemorrhage or bleeding

Status: Terminated

Product Quantity: 1 unit

Code Information:

UDI-DI: 04953170339615 Serial number: 2501131

Distribution Pattern:

US Nationwide distribution in the state of KY.

Voluntary or Mandated:

Voluntary: Firm initiated