ENDOWRIST Adverse Event — Malfunction (MDR 2955842-2020-10345)
ENDOWRIST Adverse Event — Malfunction (MDR 2955842-2020-10345) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENDOWRIST; Generic name: FENESTRATED BIPOLAR FORCEPS; Manufacturer: INTUITIVE SURGICAL, INC.
| Device | ENDOWRIST |
|---|---|
| Generic name | FENESTRATED BIPOLAR FORCEPS |
| Manufacturer | INTUITIVE SURGICAL, INC |
| Report number | 2955842-2020-10345 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | REFER TO H10/H11 FOR FOLLOW-UP INFORMATION. |
| Source | openFDA MAUDE (device adverse events) |
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