Olympus Endoscopic Flushing Pump OFP-2 (K1001141) Recall: Intermittent Function Failure
Olympus recalls OFP-2 Endoscopic Flushing Pumps with serial numbers starting 22324666-22413929 due to intermittent function failure from internal component connection issues.
Lower-risk recall
During product testing, Olympus identified an intermittent loss of function of the OFP-2 Flushing Pump caused by an internal component connection failure.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/54174-olympus-endoscopic-flushing-pump-ofp-2-k1001141-recall-intermittent-function.
Source Summary by GovInfoNow · govinfonow.com/recall/54174-olympus-endoscopic-flushing-pump-ofp-2-k1001141-recall-intermittent-function · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0229-2025
Cite this page
“Olympus Endoscopic Flushing Pump OFP-2 (K1001141) Recall: Intermittent Function Failure.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54174-olympus-endoscopic-flushing-pump-ofp-2-k1001141-recall-intermittent-function. Based on FDA recall #Z-0229-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0229-2025%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Olympus- Category
Medical device
What to do — step by step
Check Pump Serial Number
Compare your pump's serial number to the list of affected serial numbers provided in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if my pump is affected?
The recall does not include a remedy; you should check the serial number against the list and contact Olympus for further instructions.
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Where this comes from
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.
- Official source: FDA Recall #Z-0229-2025 (August 23, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0229-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.