ESPOCAN COMBINED SPINAL + EPIDURAL ANESTHESIA TRAY Adverse Event — Malfunction (MDR 10004485)
ESPOCAN COMBINED SPINAL + EPIDURAL ANESTHESIA TRAY Adverse Event — Malfunction (MDR 10004485) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ESPOCAN COMBINED SPINAL + EPIDURAL ANESTHESIA TRAY; Generic name: ESPOCAN COMBINED SPINAL + EPIDURAL ANESTHESIA TRAY; Manufacturer: B. BR
| Device | ESPOCAN COMBINED SPINAL + EPIDURAL ANESTHESIA TRAY |
|---|---|
| Generic name | ESPOCAN COMBINED SPINAL + EPIDURAL ANESTHESIA TRAY |
| Manufacturer | B. BRAUN MEDICAL, INC. |
| Report number | 10004485 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Narrative | WHEN REMOVING EPIDURAL CATHETER POST DELIVERY NOTED CATHETER TO BE SPLIT / TORN. PORTION REMOVED FROM PT'S BACK WAS INTACT. |
| Source | openFDA MAUDE (device adverse events) |
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