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.

Olympus Corporation of the Americas Medical Device Recall: Olympus Endoscopic Flushing Pump, Model/Catalog Number: OFP-2 (K10001141) | SafeCheck