Device brand name · Coronary stent system
Multi-Link Rx Penta Coronary Stent System: medical device reports filed with FDA
228 reports name it, 2001–2006. Manufacturer given most often on reports: Guidant Vascular Intervention. Product code MAF.
- 228
- device reports naming the brand
- 0% of all MAUDE reports · about 9 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 25.4%
- classified as malfunction
- 40.4% across the product code
- 3.5%
- classified as death, as reported
- 8 reports · not verified by FDA
228 medical device reports received by FDA name the brand "Multi-Link Rx Penta Coronary Stent System" (coronary stent system); the manufacturer given most often on reports is Guidant Vascular Intervention; received from July 2001 to July 2006. 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 injury (71.1%), malfunction (25.4%) and death (3.5%); 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 replace (23.7%), difficult to remove (19.3%) and material separation (15.8%). The patient problems coded most often are therapy/non-surgical treatment, additional, intimal dissection 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 Multi-Link Rx Penta Coronary Stent System was received in the five years to August 2026; the latest was received in July 2006.
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 |
|---|---|---|---|
| Replace | 54 | 23.7% | 7.5% |
| Difficult to removethe device was hard to remove | 44 | 19.3% | 10.2% |
| Material separation | 36 | 15.8% | 3.5% |
| Difficult to insertthe device was hard to insert | 30 | 13.2% | 6.7% |
| Dislodged | 29 | 12.7% | 15.9% |
| Source, detachment from | 29 | 12.7% | 1.5% |
| Balloon rupture | 26 | 11.4% | 4.3% |
| Failure to advance | 26 | 11.4% | 20.9% |
| Sticking | 15 | 6.6% | 2.1% |
| Device, or device fragments remain in patient | 14 | 6.1% | 3.4% |
| Physical resistance | 14 | 6.1% | 2% |
| Device remains implanted | 13 | 5.7% | 6.3% |
| Deflation problem | 10 | 4.4% | 2.2% |
| Device, removal of (non-implant) | 10 | 4.4% | 2.4% |
| Difficult or delayed positioning | 10 | 4.4% | 3% |
| Difficult to position | 10 | 4.4% | 2.4% |
| Other (for use when an appropriate device code cannot be identified) | 10 | 4.4% | 3.7% |
| Tip breakage | 10 | 4.4% | 0.7% |
| Detachment of device component | 9 | 3.9% | 3.3% |
| Kinkedthe tube or line kinked | 9 | 3.9% | 1.1% |
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 |
|---|---|---|
| Therapy/non-surgical treatment, additional | 66 | 28.9% |
| Intimal dissection | 53 | 23.2% |
| Surgical procedure, additional | 34 | 14.9% |
| Foreign body, removal of | 26 | 11.4% |
| Nonresorbable materials, unretrieved in body | 23 | 10.1% |
| Perforation | 20 | 8.8% |
| Surgical procedure | 19 | 8.3% |
| Hospitalization required | 11 | 4.8% |
| Bleeding | 10 | 4.4% |
| Deaththe patient died; cause not stated by this term | 10 | 4.4% |
| Occlusion | 10 | 4.4% |
| Thrombus | 10 | 4.4% |
| Thrombosis | 9 | 3.9% |
| Treatment with medication(s) | 9 | 3.9% |
| Myocardial infarctionheart attack | 8 | 3.5% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Multi-Link Rx Penta Coronary Stent System | Product code MAF | All MAUDE reports |
|---|---|---|---|
| Reports | 228 | 23,279 | 26,136,888 |
| Share of that pool | — | 1% | 0% |
| Classified as death, per 1,000 reports | 35 | 76 | 9 |
| Classified as injury | 71.1% | 51.3% | 36.2% |
| Classified as malfunction | 25.4% | 40.4% | 62.3% |
| Filed by the manufacturer | 100% | 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% |
| Rebel | 620 | 0 | 1.8% |
| 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% |
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 Multi-Link Rx Penta Coronary Stent System reports
How many FDA reports name Multi-Link Rx Penta Coronary Stent System?
228 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?
injury (71.1%), malfunction (25.4%) and death (3.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
replace (23.7%), difficult to remove (19.3%), material separation (15.8%), difficult to insert (13.2%) and dislodged (12.7%). 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 Multi-Link Rx Penta Coronary Stent System 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.