Devices › Pump, air, non-manual, for endoscope
Device brand name · Olympus flushing pump
Flushing Pump Ofp-2 Row: medical device reports filed with FDA
380 reports name it, 2024–2026. Manufacturer given most often on reports: Keymed Medical And Industrial Equipment. Product code FEQ.
- 380
- device reports naming the brand
- 0% of all MAUDE reports · about 158 a year
- 59
- reports, 12 months to August 2026
- 139 in the 12 months before
- 99.5%
- classified as malfunction
- 97.8% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
380 medical device reports received by FDA name the brand "Flushing Pump Ofp-2 Row" (olympus flushing pump); the manufacturer given most often on reports is Keymed Medical And Industrial Equipment; received from February 2024 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
59 reports arrived in the 12 months to August 2026, down 58% from 139 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (99.5%) and injury (0.5%); across all pump, air, non-manual, for endoscope reports (product code FEQ) death is recorded in 0.1% and malfunction in 97.8%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are pumping problem (21.6%), failure to pump (14.2%) and break (13.2%). The patient problems coded most often are appropriate clinical signs, symptoms and conditions term/code not available. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 1,346 reports carrying product code FEQ. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Pumping problem | 82 | 21.6% | 17.3% |
| Failure to pump | 54 | 14.2% | 5.3% |
| Breakthe device broke | 50 | 13.2% | 10% |
| Key or button unresponsive/not working | 49 | 12.9% | 9.3% |
| Infusion or flow problema problem with flow or infusion | 17 | 4.5% | 6.4% |
| Insufficient flow or under infusion | 17 | 4.5% | 2.7% |
| Mechanical problema mechanical problem | 16 | 4.2% | 2.3% |
| Improper flow or infusion | 10 | 2.6% | 3.2% |
| Leak/splashthe device leaked | 10 | 2.6% | 8.2% |
| Loose or intermittent connection | 8 | 2.1% | 1.7% |
| Defective component | 7 | 1.8% | 0.9% |
| Activation problem | 5 | 1.3% | 0.4% |
| Connection problema connection problem | 5 | 1.3% | 1.6% |
| Excess flow or over-infusion | 5 | 1.3% | 1.9% |
| Crackthe device cracked | 4 | 1.1% | 2.5% |
| Decreased pump speed | 4 | 1.1% | 0.5% |
| Detachment of device or device componentpart of the device came off | 4 | 1.1% | 1.5% |
| Gas/air leak | 4 | 1.1% | 1.1% |
| Pressure problem | 4 | 1.1% | 1.7% |
| No device output | 3 | 0.8% | 1% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Appropriate clinical signs, symptoms and conditions term/code not available | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Flushing Pump Ofp-2 Row | Product code FEQ | All MAUDE reports |
|---|---|---|---|
| Reports | 380 | 1,346 | 26,136,888 |
| Share of that pool | — | 28.2% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 0.5% | 1.6% | 36.2% |
| Classified as malfunction | 99.5% | 97.8% | 62.3% |
| Filed by the manufacturer | 100% | 98.3% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code FEQ
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Flushing Pump Ofp-2 Jp | 322 | 79 | 0% |
| Flushing Pump Ofp-2 Us | 214 | 75 | 0% |
| Flushing Pump Ofp-2 Eu | 189 | 34 | 0% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Flushing Pump Ofp-2 Row reports
How many FDA reports name Flushing Pump Ofp-2 Row?
380 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 59 in the latest 12 months.
What kinds of events are reported?
malfunction (99.5%) and injury (0.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
pumping problem (21.6%), failure to pump (14.2%), break (13.2%), key or button unresponsive/not working (12.9%) and infusion or flow problem (4.5%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Flushing Pump Ofp-2 Row was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.