COYOTE ES Adverse Event — Malfunction (MDR 2134265-2020-05670)
COYOTE ES Adverse Event — Malfunction (MDR 2134265-2020-05670) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: COYOTE ES; Generic name: CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL; Manufacturer: BOSTON SCIENTIFIC CORPORATION.
| Device | COYOTE ES |
|---|---|
| Generic name | CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 2134265-2020-05670 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, DISTRI |
| Narrative | (B)(6). |
| Source | openFDA MAUDE (device adverse events) |
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