Class II

Medical Device Recall: Insufflation unit, UHI-4.

Olympus Corporation of the Americas · September 25, 2023

Reason for Recall

Olympus has become aware of an increased trend of both repairs and customer complaints reporting "UHI-4 stopping air supply due to the front panel LED turning off".

Distribution

Domestic: Nationwide Distribution.

States Affected

NATIONWIDE

Quantity Affected

3,172 Units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1375-2024

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.

Olympus Corporation of the Americas Medical Device Recall: Insufflation unit, UHI-4. | SafeCheck