ENDOWRIST Adverse Event — Malfunction (MDR 10000736)
ENDOWRIST Adverse Event — Malfunction (MDR 10000736) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENDOWRIST; Generic name: SYSTEM, SURGICAL, COMPUTER CONTROLLED INSTRUMENT; Manufacturer: INTUITIVE SURGICAL, INC..
| Device | ENDOWRIST |
|---|---|
| Generic name | SYSTEM, SURGICAL, COMPUTER CONTROLLED INSTRUMENT |
| Manufacturer | INTUITIVE SURGICAL, INC. |
| Report number | 10000736 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | VESSEL SEALER WOULD NOT RELEASE A TISSUE. |
| Source | openFDA MAUDE (device adverse events) |
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