XIENCE EVEROLIMUS ELUTING CORONARY STENT SYSTEM Adverse Event — Injury (MDR 2024168-2020-03932)
XIENCE EVEROLIMUS ELUTING CORONARY STENT SYSTEM Adverse Event — Injury (MDR 2024168-2020-03932) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: XIENCE EVEROLIMUS ELUTING CORONARY STENT SYSTEM; Generic name: DRUG ELUTING CORONARY STENT DELIVERY SYSTEM; Manufacturer: ABBOTT VASCUL
| Device | XIENCE EVEROLIMUS ELUTING CORONARY STENT SYSTEM |
|---|---|
| Generic name | DRUG ELUTING CORONARY STENT DELIVERY SYSTEM |
| Manufacturer | ABBOTT VASCULAR |
| Report number | 2024168-2020-03932 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | LITERATURE |
| Narrative | THIS REPORT IS BEING RESUBMITTED TO ENSURE THE ENCLOSED ATTACHMENT CAN BE EASILY OPENED BY THE FDA.NA - ATTACHMENT: [ARTICLE CN-030866.PDF]. |
| Source | openFDA MAUDE (device adverse events) |
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