Medical device recalls Moderate risk

Olympus Corporation of the Americas recalls Olympus Endoscopic Flushing Pump, Model/Catalog Number: OFP-2 (K10001141)

Recall date
August 23, 2024
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0229-2025
FDA classification
Class II
Brand / firm
Olympus Corporation of the Americas
Sold / distributed
US Nationwide distribution.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

Get recall alerts

Free email alert whenever Olympus Corporation of the Americas has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Olympus Corporation of the Americas