Class II

Medical Device Recall: Olympus Endoscopic Flushing Pump, Model/Catalog Number: OFP-2 (K10001141)

Olympus Corporation of the Americas · August 23, 2024

Reason for Recall

During product testing, Olympus identified an intermittent loss of function of the OFP-2 Flushing Pump caused by an internal component connection failure.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

445 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0229-2025

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.