Class I

Medical Device Recall: 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 treatme

Olympus Corporation of the Americas · January 16, 2026

Reason for Recall

Issue with software algorithm which may lead to overpressure events.

Product Description

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.

Distribution

Nationwide distribution

States Affected

NATIONWIDE

Quantity Affected

18 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1352-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.