ENDOWRIST Adverse Event — Malfunction (MDR 2955842-2020-10364)
ENDOWRIST Adverse Event — Malfunction (MDR 2955842-2020-10364) 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 | 2955842-2020-10364 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | OTHER |
| Narrative | ADDITIONAL INFORMATION CAN BE FOUND IN THE FOLLOWING SECTIONS: A2, A3, A4, A5, A6, G4, G7, H2, H6, H10 INTUITIVE SURGICAL, INC. (ISI) FOLLOWED UP WITH THE NURSE ON SITE AND OBTAINED THE FOLLOWING ADDITIONAL INFORMATION: THE NURSE PROVIDED THE FOLLOWING NOTES FROM THE PATIENT'S FOLLOW-UP VISIT. THE PATIENT WAS A 50-YEAR OLD MALE WHO WAS REFERRED BY HIS PRIMARY CARE PHYSICIAN FOR EVALUATION OF A REN |
| Source | openFDA MAUDE (device adverse events) |
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