CYPHER SIROLIMUS-ELUTING CORONARY STENT Adverse Event — Death (MDR 3003742446-2008-00018)
CYPHER SIROLIMUS-ELUTING CORONARY STENT Adverse Event — Death (MDR 3003742446-2008-00018) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CYPHER SIROLIMUS-ELUTING CORONARY STENT; Generic name: DRUG-ELUTING STENT (NIQ); Manufacturer: CORDIS LLC (PR).
| Device | CYPHER SIROLIMUS-ELUTING CORONARY STENT |
|---|---|
| Generic name | DRUG-ELUTING STENT (NIQ) |
| Manufacturer | CORDIS LLC (PR) |
| Report number | 3003742446-2008-00018 |
| Event type | Death |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Other |
| Narrative | THIS PT HAD A STENT IMPLANTED IN THE "MAIN LEFT RENAL ARTERY" AND AN ADD'L STENT WITHIN TWO MOS. ONE OR MORE OF THE STENTS WERE TAXUS OR CYPHER. THE PT DIED TWO MOS LATER DUE TO IN-ORDINATE IN-STENT RESTENOSIS AND/OR OTHER COMPLICATIONS CAUSED BY THE "DEFECTIVE STENTS". THE DEATH CERTIFICATE LISTS THE IMMEDIATE CAUSE OF DEATH AS "ATHEROSCLEROTIC CARDIOVASCULAR DISEASE" WITH AN UNDERLYING CAUSE OF |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →