Devices › Catheters, transluminal coronary angioplasty, percutaneous
Device brand name · Catheters transluminal coronary angioplasty percutaneous
Sprinter Legend Rx: medical device reports filed with FDA
503 reports name it, 2011–2026. Manufacturer given most often on reports: Medtronic Mexico. Product code LOX.
- 503
- device reports naming the brand
- 0% of all MAUDE reports · about 34 a year
- 26
- reports, 12 months to August 2026
- 22 in the 12 months before
- 73.6%
- classified as malfunction
- 85.5% across the product code
- 1.8%
- classified as death, as reported
- 9 reports · not verified by FDA
FDA's MAUDE database holds 503 reports that name the brand "Sprinter Legend Rx" (catheters transluminal coronary angioplasty percutaneous), received between October 2011 and August 2026; the manufacturer given most often on reports is Medtronic Mexico. Spellings of one product vary from report to report.
26 reports arrived in the 12 months to August 2026, up 18% from 22 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 (73.6%), injury (24.7%) and death (1.8%); 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 burst container or vessel (36.4%), leak/splash (17.9%) and deflation problem (16.1%). The patient problems coded most often are intimal dissection, vascular dissection and device embedded in tissue or plaque. 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 |
|---|---|---|---|
| Burst container or vessel | 183 | 36.4% | 2.2% |
| Leak/splashthe device leaked | 90 | 17.9% | 2.5% |
| Deflation problem | 81 | 16.1% | 5.9% |
| Detachment of device or device componentpart of the device came off | 70 | 13.9% | 1.6% |
| Difficult to removethe device was hard to remove | 39 | 7.8% | 11.3% |
| Fracturea broken bone | 32 | 6.4% | 0.8% |
| Inflation problem | 32 | 6.4% | 5.6% |
| Material deformation | 27 | 5.4% | 1.2% |
| Improper or incorrect procedure or method | 8 | 1.6% | 4.7% |
| Difficult to open or remove packaging material | 6 | 1.2% | 0.1% |
| Breakthe device broke | 5 | 1% | 7.4% |
| Material split, cut or torn | 5 | 1% | 0.4% |
| Material distortion | 4 | 0.8% | 0% |
| Positioning problem | 4 | 0.8% | 0.1% |
| Defective devicethe device was defective | 3 | 0.6% | 0.2% |
| Difficult to position | 3 | 0.6% | 1.2% |
| Failure to advance | 3 | 0.6% | 5.4% |
| Kinkedthe tube or line kinked | 3 | 0.6% | 1.8% |
| Material rupture | 3 | 0.6% | 38.3% |
| Deformation due to compressive stress | 2 | 0.4% | 0.5% |
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 |
|---|---|---|
| Intimal dissection | 24 | 4.8% |
| Vascular dissection | 16 | 3.2% |
| Device embedded in tissue or plaque | 14 | 2.8% |
| Myocardial infarctionheart attack | 11 | 2.2% |
| Occlusion | 8 | 1.6% |
| Deaththe patient died; cause not stated by this term | 7 | 1.4% |
| Injurya physical injury | 7 | 1.4% |
| Obstruction/occlusion | 5 | 1% |
| Hemorrhage/blood loss/bleeding | 4 | 0.8% |
| Perforation | 4 | 0.8% |
| Cardiac arrestthe heart stopped | 3 | 0.6% |
| Chest painchest pain | 3 | 0.6% |
| Embolism/embolus | 3 | 0.6% |
| Ischemia | 3 | 0.6% |
| Air embolism | 2 | 0.4% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Sprinter Legend Rx | Product code LOX | All MAUDE reports |
|---|---|---|---|
| Reports | 503 | 43,618 | 26,136,888 |
| Share of that pool | — | 1.2% | 0% |
| Classified as death, per 1,000 reports | 18 | 13 | 9 |
| Classified as injury | 24.7% | 12.9% | 36.2% |
| Classified as malfunction | 73.6% | 85.5% | 62.3% |
| Filed by the manufacturer | 99.4% | 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 Sprinter Legend Rx reports
How many FDA reports name Sprinter Legend Rx?
503 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 26 in the latest 12 months.
What kinds of events are reported?
malfunction (73.6%), injury (24.7%) and death (1.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
burst container or vessel (36.4%), leak/splash (17.9%), deflation problem (16.1%), detachment of device or device component (13.9%) and difficult to remove (7.8%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.4%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Sprinter Legend Rx 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.