XIENCE DRUG ELUTING CORONARY STENT Adverse Event — Injury (MDR 2024168-2020-03944)
XIENCE DRUG ELUTING CORONARY STENT Adverse Event — Injury (MDR 2024168-2020-03944) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: XIENCE DRUG ELUTING CORONARY STENT; Generic name: DRUG ELUTING CORONARY STENT DELIVERY SYSTEM; Manufacturer: ABBOTT VASCULAR.
| Device | XIENCE DRUG ELUTING CORONARY STENT |
|---|---|
| Generic name | DRUG ELUTING CORONARY STENT DELIVERY SYSTEM |
| Manufacturer | ABBOTT VASCULAR |
| Report number | 2024168-2020-03944 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | LITERATURE |
| Narrative | (B)(4). |
| Source | openFDA MAUDE (device adverse events) |
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