Devices › Endoscopic video imaging system/component, gastroenterology-urology
Device brand name · High definition lcd monitor
High Definition Lcd Monitor: medical device reports filed with FDA
3,553 reports name it, 2017–2026. Manufacturer given most often on reports: Shirakawa Olympus. Product code FET.
- 3,553
- device reports naming the brand
- 0% of all MAUDE reports · about 374 a year
- 565
- reports, 12 months to August 2026
- 466 in the 12 months before
- 99.8%
- classified as malfunction
- 99.4% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
3,553 medical device reports received by FDA name the brand "High Definition Lcd Monitor" (high definition lcd monitor); the manufacturer given most often on reports is Shirakawa Olympus; received from January 2017 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
565 reports arrived in the 12 months to August 2026, up 21% from 466 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 (99.8%) and injury (0.2%); across all endoscopic video imaging system/component, gastroenterology-urology reports (product code FET) death is recorded in 0% and malfunction in 99.4%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are no display/image (53.4%), failure to power up (22.9%) and power problem (6.7%). The patient problems coded most often are no patient involvement, appropriate clinical signs, symptoms and conditions term/code not available and injury. 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 62,999 reports carrying product code FET. 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 |
|---|---|---|---|
| No display/image | 1,897 | 53.4% | 39.4% |
| Failure to power up | 813 | 22.9% | 2.7% |
| Power problem | 238 | 6.7% | 0.9% |
| Erratic or intermittent display | 193 | 5.4% | 5.3% |
| Electrical /electronic property probleman electrical or electronic problem | 118 | 3.3% | 1.9% |
| Loss of powerthe device lost power | 114 | 3.2% | 0.3% |
| Poor quality image | 114 | 3.2% | 16% |
| Unexpected shutdown | 84 | 2.4% | 0.3% |
| Intermittent loss of power | 57 | 1.6% | 0.2% |
| Breakthe device broke | 50 | 1.4% | 3.4% |
| Display or visual feedback problem | 47 | 1.3% | 2.2% |
| Circuit failure | 36 | 1% | 0.5% |
| Output problem | 33 | 0.9% | 3% |
| Connection problema connection problem | 21 | 0.6% | 2.5% |
| No device output | 21 | 0.6% | 0.9% |
| Defective component | 18 | 0.5% | 0.7% |
| Image display error/artifact | 12 | 0.3% | 1.2% |
| No visual prompts/feedback | 12 | 0.3% | 0.2% |
| Complete loss of power | 11 | 0.3% | 0.1% |
| Electrical power problem | 9 | 0.3% | 0.1% |
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 |
|---|---|---|
| No patient involvement | 122 | 3.4% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 3 | 0.1% |
| Injurya physical injury | 2 | 0.1% |
| Bone cement implantation syndrome | 1 | 0% |
| Perforation | 1 | 0% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | High Definition Lcd Monitor | Product code FET | All MAUDE reports |
|---|---|---|---|
| Reports | 3,553 | 62,999 | 26,136,888 |
| Share of that pool | — | 5.6% | 0% |
| Classified as death, per 1,000 reports | 0 | 0 | 9 |
| Classified as injury | 0.2% | 0.6% | 36.2% |
| Classified as malfunction | 99.8% | 99.4% | 62.3% |
| Filed by the manufacturer | 100% | 99.8% | 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 FET
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Hd Camera Head | 8,629 | 2,603 | 0% |
| Hd Autoclavable Camera Head | 7,648 | 1,554 | 0% |
| 4k Camera Head | 5,453 | 1,701 | 0% |
| Camera Head | 3,771 | 948 | 0% |
| 4k Autoclavable Camera Head | 3,098 | 723 | 0% |
| Video System Center | 3,431 | 838 | 0% |
| Visera Elite Video System Center | 2,688 | 572 | 0% |
| Hd 3cmos Autoclavable Camera Head | 2,118 | 727 | 0% |
| Visera 4k Uhd Camera Control Unit | 1,860 | 425 | 0% |
| Evis X1 Video System Center | 1,424 | 858 | 0% |
| Hd 3cmos Camera Head | 1,502 | 572 | 0% |
| Evis Lucera Elite Video System Center | 1,347 | 554 | 0% |
| VISERA Pro VIDEO SYSTEM CENTER | 637 | 96 | 0% |
| Video System | 558 | 73 | 0% |
| Visera Video System Center | 341 | 73 | 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 High Definition Lcd Monitor reports
How many FDA reports name High Definition Lcd Monitor?
3,553 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 565 in the latest 12 months.
What kinds of events are reported?
malfunction (99.8%) and injury (0.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
no display/image (53.4%), failure to power up (22.9%), power problem (6.7%), erratic or intermittent display (5.4%) and electrical /electronic property problem (3.3%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%) and distributor reports (0%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that High Definition Lcd Monitor 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.