Devices › Catheters, transluminal coronary angioplasty, percutaneous
Device brand name · Coronary dilatation catheter
Mini Trek Coronary Dilatation Catheter: medical device reports filed with FDA
1,538 reports name it, 2010–2024. Manufacturer given most often on reports: Av-Temecula-Ct. Product code LOX.
- 1,538
- device reports naming the brand
- 0% of all MAUDE reports · about 95 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 93.8%
- classified as malfunction
- 85.5% across the product code
- 0.5%
- classified as death, as reported
- 8 reports · not verified by FDA
1,538 medical device reports received by FDA name the brand "Mini Trek Coronary Dilatation Catheter" (coronary dilatation catheter); the manufacturer given most often on reports is Av-Temecula-Ct; received from May 2010 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 (93.8%), injury (5.7%) and death (0.5%); across all catheters, transluminal coronary angioplasty, percutaneous reports (product code LOX) death is recorded in 1.3% and malfunction in 85.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are material rupture (55.7%), difficult to remove (19.3%) and improper or incorrect procedure or method (16%). The patient problems coded most often are no patient involvement, intimal dissection and myocardial infarction. 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 43,618 reports carrying product code LOX. 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 rupture | 857 | 55.7% | 38.3% |
| Difficult to removethe device was hard to remove | 297 | 19.3% | 11.3% |
| Improper or incorrect procedure or method | 246 | 16% | 4.7% |
| Physical resistance | 181 | 11.8% | 2.3% |
| Detachment of device component | 149 | 9.7% | 4.3% |
| Inflation problem | 147 | 9.6% | 5.6% |
| Failure to advance | 118 | 7.7% | 5.4% |
| Difficult to advance | 113 | 7.3% | 3.5% |
| Leak/splashthe device leaked | 82 | 5.3% | 2.5% |
| Difficult to position | 73 | 4.7% | 1.2% |
| Material separation | 51 | 3.3% | 3% |
| Deflation problem | 45 | 2.9% | 5.9% |
| Kinkedthe tube or line kinked | 39 | 2.5% | 1.8% |
| Torn material | 36 | 2.3% | 0.4% |
| Deformation due to compressive stress | 17 | 1.1% | 0.5% |
| Material split, cut or torn | 17 | 1.1% | 0.4% |
| Breakthe device broke | 11 | 0.7% | 7.4% |
| Folded | 6 | 0.4% | 0.3% |
| Crackthe device cracked | 4 | 0.3% | 0.1% |
| Off-label use | 4 | 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 | 91 | 5.9% |
| Intimal dissection | 28 | 1.8% |
| Myocardial infarctionheart attack | 9 | 0.6% |
| Non specific ekg/ECG changes | 9 | 0.6% |
| Perforation | 9 | 0.6% |
| Angina | 8 | 0.5% |
| Cardiac arrestthe heart stopped | 8 | 0.5% |
| Arrhythmia | 7 | 0.5% |
| Occlusion | 7 | 0.5% |
| Air embolism | 6 | 0.4% |
| Deaththe patient died; cause not stated by this term | 6 | 0.4% |
| Foreign body in patientpart of a device left in the patient | 6 | 0.4% |
| Ischemia | 6 | 0.4% |
| Low blood pressure/ hypotension | 6 | 0.4% |
| Perforation of vessels | 5 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Mini Trek Coronary Dilatation Catheter | Product code LOX | All MAUDE reports |
|---|---|---|---|
| Reports | 1,538 | 43,618 | 26,136,888 |
| Share of that pool | — | 3.5% | 0% |
| Classified as death, per 1,000 reports | 5 | 13 | 9 |
| Classified as injury | 5.7% | 12.9% | 36.2% |
| Classified as malfunction | 93.8% | 85.5% | 62.3% |
| Filed by the manufacturer | 99.9% | 97.7% | 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 LOX
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| NC Emerge | 5,690 | 543 | 1.4% |
| Nc Trek Coronary Dilatation Catheter | 4,689 | 0 | 0.5% |
| Emerge | 3,724 | 168 | 1.8% |
| NC Quantum Apex? | 2,518 | 30 | 0.8% |
| Trek Coronary Dilatation Catheter | 2,204 | 3 | 1.1% |
| Maverick2 Monorail Ptca Catheter | 1,579 | 0 | 1.1% |
| Maverick? | 1,337 | 71 | 0.4% |
| Ptca Catheters | 1,269 | 0 | 0.4% |
| Quantum? Maverick? | 1,173 | 39 | 0.3% |
| Voyager Nc Coronary Dilatation Catheter | 747 | 0 | 0.5% |
| Apex Monorail | 603 | 0 | 1.7% |
| Euphora Rx | 529 | 43 | 1.7% |
| Voyager Rx Coronary Dilatation Catheter | 736 | 0 | 0.7% |
| Apex | 876 | 78 | 1.3% |
| Nc Traveler Coronary Dilatation Catheter | 504 | 0 | 0.6% |
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 Mini Trek Coronary Dilatation Catheter reports
How many FDA reports name Mini Trek Coronary Dilatation Catheter?
1,538 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 (93.8%), injury (5.7%) 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 rupture (55.7%), difficult to remove (19.3%), improper or incorrect procedure or method (16%), physical resistance (11.8%) and detachment of device component (9.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.9%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Mini Trek Coronary Dilatation Catheter 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.