Device brand name · Stent coronary
Rebel: medical device reports filed with FDA
620 reports name it, 2014–2022. Manufacturer given most often on reports: Boston Scientific - Maple Grove. Product code MAF.
- 620
- device reports naming the brand
- 0% of all MAUDE reports · about 52 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 82.7%
- classified as malfunction
- 40.4% across the product code
- 1.8%
- classified as death, as reported
- 11 reports · not verified by FDA
FDA's MAUDE database holds 620 reports that name the brand "Rebel" (stent coronary), received between September 2014 and November 2022; the manufacturer given most often on reports is Boston Scientific - Maple Grove. 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 (82.7%), injury (15.5%) and death (1.8%); across all stent, coronary reports (product code MAF) death is recorded in 7.6% and malfunction in 40.4%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are bent (23.5%), material deformation (22.1%) and failure to advance (19%). The patient problems coded most often are no patient involvement, device embedded in tissue or plaque and death. 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 23,279 reports carrying product code MAF. 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 |
|---|---|---|---|
| Bent | 146 | 23.5% | 3.6% |
| Material deformation | 137 | 22.1% | 3% |
| Failure to advance | 118 | 19% | 20.9% |
| Device dislodged or dislocated | 99 | 16% | 7% |
| Breakthe device broke | 54 | 8.7% | 2.2% |
| Device damaged prior to usethe device was damaged before use | 52 | 8.4% | 3.8% |
| Difficult to removethe device was hard to remove | 24 | 3.9% | 10.2% |
| Fracturea broken bone | 18 | 2.9% | 1% |
| Occlusion within devicethe device blocked | 13 | 2.1% | 4.7% |
| Device damaged by another device | 12 | 1.9% | 0.3% |
| Material rupture | 10 | 1.6% | 0.8% |
| Difficult to advance | 9 | 1.5% | 0.7% |
| Activation, positioning or separation problem | 8 | 1.3% | 0.3% |
| Entrapment of device | 7 | 1.1% | 0.6% |
| Defective devicethe device was defective | 5 | 0.8% | 0.2% |
| Material twisted/bent | 5 | 0.8% | 0.1% |
| Deflation problem | 3 | 0.5% | 2.2% |
| Kinkedthe tube or line kinked | 3 | 0.5% | 1.1% |
| Migration or expulsion of device | 3 | 0.5% | 2.5% |
| Component missing | 2 | 0.3% | 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 |
|---|---|---|
| No patient involvement | 90 | 14.5% |
| Device embedded in tissue or plaque | 11 | 1.8% |
| Deaththe patient died; cause not stated by this term | 10 | 1.6% |
| Thrombosis | 10 | 1.6% |
| Myocardial infarctionheart attack | 9 | 1.5% |
| Chest painchest pain | 8 | 1.3% |
| Intimal dissection | 4 | 0.6% |
| Cardiac enzyme elevation | 3 | 0.5% |
| Low blood pressure/ hypotension | 3 | 0.5% |
| Reocclusion | 3 | 0.5% |
| Stenosis | 3 | 0.5% |
| Foreign body in patientpart of a device left in the patient | 2 | 0.3% |
| Non specific ekg/ECG changes | 2 | 0.3% |
| Anemialow red blood cells | 1 | 0.2% |
| Cardiac arrestthe heart stopped | 1 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Rebel | Product code MAF | All MAUDE reports |
|---|---|---|---|
| Reports | 620 | 23,279 | 26,136,888 |
| Share of that pool | — | 2.7% | 0% |
| Classified as death, per 1,000 reports | 18 | 76 | 9 |
| Classified as injury | 15.5% | 51.3% | 36.2% |
| Classified as malfunction | 82.7% | 40.4% | 62.3% |
| Filed by the manufacturer | 99.2% | 95.6% | 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 MAF
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Graftmaster Rx Coronary Stent Graft System | 2,163 | 0 | 13.1% |
| Multi-Link Rx Vision Coronary Stent System | 1,875 | 0 | 4.2% |
| Jostent Graftmaster | 1,373 | 0 | 23.5% |
| Express2 Monorail Coronary Stent Delivery System | 881 | 0 | 2.5% |
| Multi-Link Mini Vision Rx Coronary Stent System | 867 | 0 | 4.7% |
| Liberte' Monorail Coronary Stent Delivery System | 802 | 0 | 3.4% |
| Multi-Link 8 | 621 | 1 | 1.6% |
| Veriflex Liberte Coronary Stent Delivery System | 603 | 0 | 18.6% |
| Integrity Rx | 533 | 0 | 8.4% |
| Graftmaster | 568 | 131 | 9.9% |
| Libert | 415 | 0 | 0.7% |
| Omega | 353 | 0 | 1.4% |
| Multi-Link Rx Zeta Coronary Stent System | 351 | 0 | 6.6% |
| Acs Rx Multi-Link Coronary Stent System | 327 | 6 | 6.1% |
| Multi-Link Rx Pixel Coronary Stent System | 326 | 0 | 4.3% |
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 Rebel reports
How many FDA reports name Rebel?
620 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 (82.7%), injury (15.5%) and death (1.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
bent (23.5%), material deformation (22.1%), failure to advance (19%), device dislodged or dislocated (16%) and break (8.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.2%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Rebel 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.