PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: November 6, 2024 Initiated: August 23, 2024 #Z-0229-2025

Product Description

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

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.

Details

Units Affected
445 units
Distribution
US Nationwide distribution.
Location
Center Valley, PA

Frequently Asked Questions

What product was recalled?
Olympus Endoscopic Flushing Pump, Model/Catalog Number: OFP-2 (K10001141). Recalled by Olympus Corporation of the Americas. Units affected: 445 units.
Why was this product recalled?
During product testing, Olympus identified an intermittent loss of function of the OFP-2 Flushing Pump caused by an internal component connection failure.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 6, 2024. Severity: Moderate. Recall number: Z-0229-2025.