Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic

Recalled February 25, 2026 · FDA recall Z-1352-2026 · Olympus Corporation of the Americas

Hazard

Issue with software algorithm which may lead to overpressure events. · FDA Class I

Units

18 units

Sold at

Nationwide distribution

Description

Issue with software algorithm which may lead to overpressure events.

Product

Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.

Manufacturer(s)

Olympus Corporation of the Americas

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →