Devices › Laparoscope, general & plastic surgery
Device brand name · Gcj
Ctf73 12x100 Kii Fios Zthr 6/Bx: medical device reports filed with FDA
201 reports name it, 2015–2024. Manufacturer given most often on reports: Applied Medical Resources. Product code GCJ.
- 201
- device reports naming the brand
- 0% of all MAUDE reports · about 18 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 94.5%
- classified as malfunction
- 90.1% across the product code
- 0.5%
- classified as death, as reported
- 1 reports · not verified by FDA
201 medical device reports received by FDA name the brand "Ctf73 12x100 Kii Fios Zthr 6/Bx" (gcj); the manufacturer given most often on reports is Applied Medical Resources; received from April 2015 to June 2024. 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 (94.5%), injury (5%) and death (0.5%); across all laparoscope, general & plastic surgery reports (product code GCJ) death is recorded in 0.3% and malfunction in 90.1%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are material fragmentation (36.8%), break (18.4%) and detachment of device or device component (11.9%). The patient problems coded most often are foreign body in patient, injury and bowel perforation. 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 84,093 reports carrying product code GCJ. 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 |
|---|---|---|---|
| Material fragmentation | 74 | 36.8% | 2.4% |
| Breakthe device broke | 37 | 18.4% | 13.5% |
| Detachment of device or device componentpart of the device came off | 24 | 11.9% | 6% |
| Detachment of device component | 15 | 7.5% | 5.3% |
| Fracturea broken bone | 11 | 5.5% | 0.5% |
| Device contaminated during manufacture or shipping | 3 | 1.5% | 0.2% |
| Physical resistance | 3 | 1.5% | 0.1% |
| Physical resistance/sticking | 3 | 1.5% | 0.1% |
| Ambient noise problem | 2 | 1% | 0% |
| Component falling | 2 | 1% | 1.6% |
| Contamination /decontamination problem | 2 | 1% | 0.1% |
| Gas/air leak | 2 | 1% | 1.7% |
| Material split, cut or torn | 2 | 1% | 2.5% |
| Bent | 1 | 0.5% | 0.3% |
| Crackthe device cracked | 1 | 0.5% | 1.5% |
| Defective devicethe device was defective | 1 | 0.5% | 0.3% |
| Device dislodged or dislocated | 1 | 0.5% | 0.4% |
| Device operates differently than expectedthe device behaved unexpectedly | 1 | 0.5% | 1% |
| Entrapment of device | 1 | 0.5% | 0.2% |
| Fogging | 1 | 0.5% | 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 |
|---|---|---|
| Foreign body in patientpart of a device left in the patient | 3 | 1.5% |
| Injurya physical injury | 3 | 1.5% |
| Bowel perforation | 2 | 1% |
| Device embedded in tissue or plaque | 2 | 1% |
| Post operative wound infection | 2 | 1% |
| Blood loss | 1 | 0.5% |
| Complaint, ill-defined | 1 | 0.5% |
| Deaththe patient died; cause not stated by this term | 1 | 0.5% |
| Discomfortdiscomfort | 1 | 0.5% |
| Great vessel perforation | 1 | 0.5% |
| Hemorrhage/blood loss/bleeding | 1 | 0.5% |
| Hernia | 1 | 0.5% |
| Internal organ perforation | 1 | 0.5% |
| No patient involvement | 1 | 0.5% |
| Perforation of vessels | 1 | 0.5% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Ctf73 12x100 Kii Fios Zthr 6/Bx | Product code GCJ | All MAUDE reports |
|---|---|---|---|
| Reports | 201 | 84,093 | 26,136,888 |
| Share of that pool | — | 0.2% | 0% |
| Classified as death, per 1,000 reports | 5 | 3 | 9 |
| Classified as injury | 5% | 8.3% | 36.2% |
| Classified as malfunction | 94.5% | 90.1% | 62.3% |
| Filed by the manufacturer | 100% | 94.8% | 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 GCJ
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Endoeye Flex Deflectable Videoscope | 8,062 | 2,245 | 0% |
| Auto Suture | 3,100 | 234 | 0.1% |
| Endopath Dilating Tip Trocar | 2,475 | 0 | 0.4% |
| VersaOne | 1,890 | 251 | 0.2% |
| Endoeye Flex 3d Deflectable Videoscope | 1,825 | 711 | 0% |
| Spacemaker | 1,379 | 146 | 0% |
| Versaport | 1,198 | 64 | 0.1% |
| Endopath Disposable Surgical Trocar | 1,153 | 0 | 0.4% |
| Pdb | 1,253 | 180 | 0% |
| Endopath Xcel Bladeless Trocar | 986 | 28 | 0.3% |
| Auto Suture Multifire Endo Gia 30-2 5 | 933 | 0 | 0% |
| Endopath Xcel Trocar | 844 | 0 | 0.9% |
| Lapro-Clip | 856 | 54 | 0.2% |
| Auto Suture Endo Clip 5mm | 795 | 0 | 0% |
| Endopath Xcel | 786 | 38 | 0.5% |
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 Ctf73 12x100 Kii Fios Zthr 6/Bx reports
How many FDA reports name Ctf73 12x100 Kii Fios Zthr 6/Bx?
201 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 (94.5%), injury (5%) and death (0.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
material fragmentation (36.8%), break (18.4%), detachment of device or device component (11.9%), detachment of device component (7.5%) and fracture (5.5%). 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 Ctf73 12x100 Kii Fios Zthr 6/Bx 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.