Devices › Light source, fiberoptic, routine
Device brand name · Lightsource
L9000 Lightsource: medical device reports filed with FDA
385 reports name it, 2009–2012. Manufacturer given most often on reports: Stryker Endoscopy San Jose. Product code FCW.
- 385
- device reports naming the brand
- 0% of all MAUDE reports · about 23 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 99.2%
- classified as malfunction
- 94.2% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
385 medical device reports received by FDA name the brand "L9000 Lightsource" (lightsource); the manufacturer given most often on reports is Stryker Endoscopy San Jose; received from October 2009 to August 2012. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
0 reports arrived in the 12 months to August 2026, and none 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 (99.2%) and injury (0.8%); across all light source, fiberoptic, routine reports (product code FCW) death is recorded in 0% and malfunction in 94.2%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are device displays incorrect message (46.2%), device operates differently than expected (17.7%) and loss of power (8.8%). The patient problems coded most often are no patient involvement, burn, thermal and burn(s). 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
No report naming L9000 Lightsource was received in the five years to August 2026; the latest was received in August 2012.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 2,970 reports carrying product code FCW. 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 |
|---|---|---|---|
| Device displays incorrect message | 178 | 46.2% | 25.7% |
| Device operates differently than expectedthe device behaved unexpectedly | 68 | 17.7% | 7.2% |
| Loss of powerthe device lost power | 34 | 8.8% | 6.6% |
| Application interface becomes non-functional or program exits abnormally | 32 | 8.3% | 5.1% |
| Device stops intermittentlythe device stopped now and then | 24 | 6.2% | 1.8% |
| Optical problem | 18 | 4.7% | 4.4% |
| Failure to power up | 16 | 4.2% | 3.3% |
| Device inoperablethe device could not be used | 14 | 3.6% | 1.8% |
| Self-activation or keying | 12 | 3.1% | 1.3% |
| Sticking | 6 | 1.6% | 0.6% |
| Image display error/artifact | 5 | 1.3% | 0.1% |
| Out-of-box failure | 4 | 1% | 0.3% |
| Computer software problema software problem | 3 | 0.8% | 0.3% |
| No device output | 3 | 0.8% | 0.6% |
| Thermal decomposition of device | 3 | 0.8% | 2.7% |
| Device emits odor | 2 | 0.5% | 3.1% |
| Device slipped | 2 | 0.5% | 0.1% |
| Improper or incorrect procedure or method | 2 | 0.5% | 0.3% |
| No display/image | 2 | 0.5% | 1.7% |
| Detachment of device component | 1 | 0.3% | 0.2% |
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 | 4 | 1% |
| Burn, thermal | 2 | 0.5% |
| Burn(s)a burn | 1 | 0.3% |
| Erythemaskin redness | 1 | 0.3% |
| Full thickness (third degree) burn | 1 | 0.3% |
| Swellingswelling | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | L9000 Lightsource | Product code FCW | All MAUDE reports |
|---|---|---|---|
| Reports | 385 | 2,970 | 26,136,888 |
| Share of that pool | — | 13% | 0% |
| Classified as death, per 1,000 reports | 0 | 0 | 9 |
| Classified as injury | 0.8% | 5.1% | 36.2% |
| Classified as malfunction | 99.2% | 94.2% | 62.3% |
| Filed by the manufacturer | 100% | 96.5% | 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 FCW
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| X8000 Lightsource | 963 | 0 | 0% |
| Mlx 300w Xenon Lightsource | 558 | 36 | 0% |
| X7000 Xenon Lightsource | 321 | 0 | 0% |
| All-In-One Ccu+light Row | 256 | 75 | 0% |
| Unknown_Endoscopy_Product | 241 | 22 | 0.4% |
| Mayfield Ultra Base Unit | 495 | 8 | 0% |
| Pentax | 47,288 | 2,443 | 0.1% |
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 L9000 Lightsource reports
How many FDA reports name L9000 Lightsource?
385 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
malfunction (99.2%) and injury (0.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device displays incorrect message (46.2%), device operates differently than expected (17.7%), loss of power (8.8%), application interface becomes non-functional or program exits abnormally (8.3%) and device stops intermittently (6.2%). 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 L9000 Lightsource 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.