UNKNOWN KNEE TIBIAL TRAY Adverse Event — Malfunction (MDR 1818910-2020-11408)
UNKNOWN KNEE TIBIAL TRAY Adverse Event — Malfunction (MDR 1818910-2020-11408) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN KNEE TIBIAL TRAY; Generic name: KNEE TIBIAL TRAY; Manufacturer: DEPUY ORTHOPAEDICS INC US.
| Device | UNKNOWN KNEE TIBIAL TRAY |
|---|---|
| Generic name | KNEE TIBIAL TRAY |
| Manufacturer | DEPUY ORTHOPAEDICS INC US |
| Report number | 1818910-2020-11408 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, HEALTH PROFESSIONAL, L |
| Narrative | DEPUY SYNTHES IS SUBMITTING THIS REPORT PURSUANT TO THE PROVISION OF 21 CFR, PART 803. THE REPORT MAY BE BASED ON THE INFORMATION WHICH DEPUY SYNTHES HAS NOT BEEN ABLE TO INVESTIGATE OR VERIFY PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY FDA, DEPUY SYNTHES OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE DEVICE, DEPUY SYNTHES, OR ITS EMPLOYEE |
| Source | openFDA MAUDE (device adverse events) |
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