UNK KNEE IMPACTOR Adverse Event — Malfunction (MDR 1818910-2020-11384)
UNK KNEE IMPACTOR Adverse Event — Malfunction (MDR 1818910-2020-11384) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNK KNEE IMPACTOR; Generic name: KNEE IMPACTOR; Manufacturer: DEPUY ORTHOPAEDICS INC US.
| Device | UNK KNEE IMPACTOR |
|---|---|
| Generic name | KNEE IMPACTOR |
| Manufacturer | DEPUY ORTHOPAEDICS INC US |
| Report number | 1818910-2020-11384 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | Foreign, Health Professional, Company representation |
| Narrative | PRODUCT COMPLAINT#: (B)(4). DEPUY SYNTHES IS SUBMITTING THIS REPORT PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803. THIS REPORT MAY BE BASED ON 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, DEPU |
| Source | openFDA MAUDE (device adverse events) |
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