Devices › Duodenoscope and accessories, flexible/rigid
Device brand name · Duodenovideoscope
Evis Lucera Duodenovideoscope: medical device reports filed with FDA
3,630 reports name it, 2017–2026. Manufacturer given most often on reports: Aizu Olympus. Product code FDT.
- 3,630
- device reports naming the brand
- 0% of all MAUDE reports · about 415 a year
- 1,681
- reports, 12 months to August 2026
- 392 in the 12 months before
- 89%
- classified as malfunction
- 88.5% across the product code
- 0.8%
- classified as death, as reported
- 30 reports · not verified by FDA
FDA's MAUDE database holds 3,630 reports that name the brand "Evis Lucera Duodenovideoscope" (duodenovideoscope), received between October 2017 and August 2026; the manufacturer given most often on reports is Aizu Olympus. Spellings of one product vary from report to report.
1,681 reports arrived in the 12 months to August 2026, up 329% from 392 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 (89%), injury (10.2%) and death (0.8%); across all duodenoscope and accessories, flexible/rigid reports (product code FDT) death is recorded in 0.7% and malfunction in 88.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are peeled/delaminated (30.3%), failure to clean adequately (13.1%) and crack (6.8%). The patient problems coded most often are pancreatitis, hemorrhage/blood loss/bleeding and inflammation. 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 25,159 reports carrying product code FDT. 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 |
|---|---|---|---|
| Peeled/delaminated | 1,100 | 30.3% | 9.2% |
| Failure to clean adequately | 476 | 13.1% | 16.9% |
| Crackthe device cracked | 247 | 6.8% | 9.6% |
| Breakthe device broke | 202 | 5.6% | 6.3% |
| Detachment of device or device componentpart of the device came off | 163 | 4.5% | 9.3% |
| Residue after decontamination | 133 | 3.7% | 2.2% |
| Flare or flash | 125 | 3.4% | 1% |
| Thermal decomposition of device | 122 | 3.4% | 0.9% |
| Device reprocessing problem | 118 | 3.3% | 6.8% |
| Contamination | 111 | 3.1% | 3% |
| Microbial contamination of device | 104 | 2.9% | 8.8% |
| Device contamination with chemical or other material | 89 | 2.5% | 1.4% |
| Material fragmentation | 85 | 2.3% | 1.8% |
| Material split, cut or torn | 85 | 2.3% | 1.5% |
| Material discolored | 80 | 2.2% | 1.3% |
| Melted | 78 | 2.1% | 0.6% |
| Degraded | 73 | 2% | 3.5% |
| Corrodedthe device corroded | 64 | 1.8% | 2.5% |
| Mechanical problema mechanical problem | 55 | 1.5% | 1.2% |
| Overheating of device | 53 | 1.5% | 0.4% |
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 |
|---|---|---|
| Pancreatitisinflammation of the pancreas | 129 | 3.6% |
| Hemorrhage/blood loss/bleeding | 79 | 2.2% |
| Inflammationinflammation | 56 | 1.5% |
| Cholangitis | 52 | 1.4% |
| Perforation | 52 | 1.4% |
| Injurya physical injury | 43 | 1.2% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 18 | 0.5% |
| Abdominal painstomach or belly pain | 14 | 0.4% |
| Bacterial infectiona bacterial infection | 13 | 0.4% |
| Sepsisa severe body-wide response to infection | 12 | 0.3% |
| Pneumonialung infection | 11 | 0.3% |
| Bowel perforation | 8 | 0.2% |
| Fever | 8 | 0.2% |
| Gastrointestinal hemorrhage | 7 | 0.2% |
| Foreign body in patientpart of a device left in the patient | 6 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Evis Lucera Duodenovideoscope | Product code FDT | All MAUDE reports |
|---|---|---|---|
| Reports | 3,630 | 25,159 | 26,136,888 |
| Share of that pool | — | 14.4% | 0% |
| Classified as death, per 1,000 reports | 8 | 7 | 9 |
| Classified as injury | 10.2% | 10.5% | 36.2% |
| Classified as malfunction | 89% | 88.5% | 62.3% |
| Filed by the manufacturer | 100% | 97.6% | 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 FDT
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Pentax | 47,288 | 2,443 | 0.1% |
| Evis Lucera Elite Duodenovideoscope | 1,370 | 882 | 0.2% |
| Single Use Distal Cover | 1,025 | 102 | 0% |
| Evis Exera Duodenovideoscope | 966 | 74 | 2% |
| Duodenovideoscope | 874 | 289 | 0.7% |
| EXALT Model D Single-Use Duodenoscope | 306 | 39 | 0.7% |
| CRE Wireguided | 718 | 56 | 0.3% |
| Olympus | 2,240 | 9 | 2.5% |
| Single Use Ligating Device | 594 | 170 | 0% |
| THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip | 1,505 | 38 | 0.3% |
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 Evis Lucera Duodenovideoscope reports
How many FDA reports name Evis Lucera Duodenovideoscope?
3,630 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 1,681 in the latest 12 months.
What kinds of events are reported?
malfunction (89%), injury (10.2%) and death (0.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
peeled/delaminated (30.3%), failure to clean adequately (13.1%), crack (6.8%), break (5.6%) and detachment of device or device component (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 Evis Lucera Duodenovideoscope 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.