Devices › Catheters, transluminal coronary angioplasty, percutaneous
Device brand name · Ptca catheter
Adante Catheter: medical device reports filed with FDA
191 reports name it, 1999–2002. Manufacturer given most often on reports: Boston Scientific Ireland. Product code LOX.
- 191
- device reports naming the brand
- 0% of all MAUDE reports · about 7 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 87.4%
- classified as malfunction
- 85.5% across the product code
- 0.5%
- classified as death, as reported
- 1 reports · not verified by FDA
FDA's MAUDE database holds 191 reports that name the brand "Adante Catheter" (ptca catheter), received between August 1999 and September 2002; the manufacturer given most often on reports is Boston Scientific Ireland. Spellings of one product vary from report to report.
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 (87.4%), injury (12%) 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 shaft break (50.3%), break (38.7%) and difficult to insert (23%). The patient problems coded most often are foreign body, removal of, surgical procedure and surgical procedure, additional. 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 Adante Catheter was received in the five years to August 2026; the latest was received in September 2002.
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 |
|---|---|---|---|
| Shaft break | 96 | 50.3% | 1.9% |
| Breakthe device broke | 74 | 38.7% | 7.4% |
| Difficult to insertthe device was hard to insert | 44 | 23% | 1.2% |
| Device, removal of (non-implant) | 34 | 17.8% | 2.2% |
| Difficult to removethe device was hard to remove | 27 | 14.1% | 11.3% |
| Component(s), broken | 21 | 11% | 0.2% |
| Kinkedthe tube or line kinked | 14 | 7.3% | 1.8% |
| Failure to advance | 12 | 6.3% | 5.4% |
| Material separation | 12 | 6.3% | 3% |
| Inflation problem | 8 | 4.2% | 5.6% |
| Deflation problem | 7 | 3.7% | 5.9% |
| Replace | 7 | 3.7% | 4.8% |
| Bent | 6 | 3.1% | 0.1% |
| Balloon rupture | 5 | 2.6% | 10.2% |
| Device, or device fragments remain in patient | 5 | 2.6% | 0.5% |
| Out-of-box failure | 5 | 2.6% | 0.1% |
| Sticking | 5 | 2.6% | 0.7% |
| Difficult to position | 4 | 2.1% | 1.2% |
| Difficult or delayed positioning | 2 | 1% | 0.1% |
| Entrapment of device | 2 | 1% | 1.5% |
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, removal of | 29 | 15.2% |
| Surgical procedure | 8 | 4.2% |
| Surgical procedure, additional | 4 | 2.1% |
| Other (for use when an appropriate patient code cannot be identified) | 3 | 1.6% |
| Therapy/non-surgical treatment, additional | 3 | 1.6% |
| Nonresorbable materials, unretrieved in body | 2 | 1% |
| Angina | 1 | 0.5% |
| Cardiac arrestthe heart stopped | 1 | 0.5% |
| Chest painchest pain | 1 | 0.5% |
| Deaththe patient died; cause not stated by this term | 1 | 0.5% |
| Intimal dissection | 1 | 0.5% |
| Muscle spasm(s) | 1 | 0.5% |
| Myocardial infarctionheart attack | 1 | 0.5% |
| Resuscitation | 1 | 0.5% |
| Treatment with medication(s) | 1 | 0.5% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Adante Catheter | Product code LOX | All MAUDE reports |
|---|---|---|---|
| Reports | 191 | 43,618 | 26,136,888 |
| Share of that pool | — | 0.4% | 0% |
| Classified as death, per 1,000 reports | 5 | 13 | 9 |
| Classified as injury | 12% | 12.9% | 36.2% |
| Classified as malfunction | 87.4% | 85.5% | 62.3% |
| Filed by the manufacturer | 100% | 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% |
| Mini Trek Coronary Dilatation Catheter | 1,538 | 0 | 0.5% |
| 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% |
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 Adante Catheter reports
How many FDA reports name Adante Catheter?
191 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 (87.4%), injury (12%) and death (0.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
shaft break (50.3%), break (38.7%), difficult to insert (23%), device, removal of (non-implant) (17.8%) and difficult to remove (14.1%). 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 Adante 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.