Olympus recalls OFP-2 Endoscopic Flushing Pumps with serial numbers starting 22324666-22413929 due to intermittent function failure from internal component connection issues.
During product testing, Olympus identified an intermittent loss of function of the OFP-2 Flushing Pump caused by an internal component connection failure.
Olympus is recalling endoscopic flushing pumps model OFP-2 (K10001141) because testing found they can sometimes stop working due to a connection failure inside the pump. This could lead to inconsistent fluid flow during medical procedures.
During testing, Olympus identified that the pump's internal connection can fail intermittently, causing the pump to lose function. This may result in inconsistent fluid flow during medical procedures, but the hazard does not involve immediate danger like fire or injury.
Medical professionals using Olympus Endoscopic Flushing Pumps model OFP-2 (K10001141) with the listed serial numbers are most at risk. The recall affects specific units sold in the U.S. market.
Check if your pump has the model number OFP-2 (K10001141) and one of the listed serial numbers from the provided list. The recall covers specific units sold in the U.S.
Compare your pump's serial number to the list of affected serial numbers provided in the recall notice.
Olympus identified an intermittent loss of function in the OFP-2 Flushing Pump during testing due to an internal component connection failure.
Check if your pump has the model number OFP-2 (K10001141) and a serial number from the list of affected serial numbers provided in the recall notice.
The recall does not include a remedy; you should check the serial number against the list and contact Olympus for further instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0229-2025 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0229-2025 from Olympus. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
