ENDOWRIST Adverse Event — Malfunction (MDR 2955842-2020-10383)
ENDOWRIST Adverse Event — Malfunction (MDR 2955842-2020-10383) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENDOWRIST; Generic name: MONOPOLAR CURVED SCISSORS; Manufacturer: INTUITIVE SURGICAL, INC.
| Device | ENDOWRIST |
|---|---|
| Generic name | MONOPOLAR CURVED SCISSORS |
| Manufacturer | INTUITIVE SURGICAL, INC |
| Report number | 2955842-2020-10383 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | OTHER |
| Narrative | THE MONOPOLAR CURVED SCISSORS INSTRUMENT HAD A BROKEN CONDUCTOR WIRE. FA REMOVED THE HOUSING AND THE CONDUCTOR WIRE WAS FOUND BROKEN INSIDE THE INSTRUMENT MAIN TUBE AT THE PROXIMAL END. THE INSTRUMENT FAILED THE ELECTRICAL CONTINUITY TEST AND THERE WERE NO SIGNS OF THERMAL DAMAGE OBSERVED. THIS COMPLAINT IS BEING REPORTED DUE TO THE FOLLOWING CONCLUSION: THE INSTRUMENT HAD CONDUCTOR WIRE DAMAGE WI |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →