EPIDURAL CATHETERIZATION KIT Adverse Event — Malfunction (MDR 1036844-2020-00133)
EPIDURAL CATHETERIZATION KIT Adverse Event — Malfunction (MDR 1036844-2020-00133) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EPIDURAL CATHETERIZATION KIT; Generic name: ANESTHESIA CONDUCTION CATHETER; Manufacturer: ARROW INTERNATIONAL INC..
| Device | EPIDURAL CATHETERIZATION KIT |
|---|---|
| Generic name | ANESTHESIA CONDUCTION CATHETER |
| Manufacturer | ARROW INTERNATIONAL INC. |
| Report number | 1036844-2020-00133 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | (B)(4). THE DEVICE HAS NOT BEEN RETURNED FOR INVESTIGATION. TELEFLEX WILL CONTINUE TO MONITOR AND TREND RELATED EVENTS. |
| Source | openFDA MAUDE (device adverse events) |
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