ARRIW Adverse Event — Malfunction (MDR 10004487)
ARRIW Adverse Event — Malfunction (MDR 10004487) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ARRIW; Generic name: EPIDURAL CATHETER; Report number: 10004487.
| Device | ARRIW |
|---|---|
| Generic name | EPIDURAL CATHETER |
| Report number | 10004487 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-17 |
| Narrative | EPIDURAL INSERTED AT 0900, PT COMFORTABLE. AT 1530 PT UNCOMFORTABLE, EPIDURAL BOLUS PLANNED. WHEN FILTER DISCONNECTED TO ADMINISTER BOLUS, CRACK NOTICED AND FILTER PROCEEDED TO BREAK APART. EPIDURAL REMOVED AND NEW CATHETER INSERTED. |
| Source | openFDA MAUDE (device adverse events) |
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