ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT Adverse Event — Malfunction (MDR 9680794-2020-00193)
ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT Adverse Event — Malfunction (MDR 9680794-2020-00193) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT; Generic name: CATHETER, EMBOLECTOMY; Manufacturer: ARROW INTERNATIONAL INC..
| Device | ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT |
|---|---|
| Generic name | CATHETER, EMBOLECTOMY |
| Manufacturer | ARROW INTERNATIONAL INC. |
| Report number | 9680794-2020-00193 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | DISTRIBUTOR, FOREIGN, HEALTH PR |
| Narrative | QN#: (B)(4). |
| Source | openFDA MAUDE (device adverse events) |
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