ADAPTER REMOVER INSTRUMENT Adverse Event — Malfunction (MDR 1818910-2020-11382)
ADAPTER REMOVER INSTRUMENT Adverse Event — Malfunction (MDR 1818910-2020-11382) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ADAPTER REMOVER INSTRUMENT; Generic name: HIP INSTRUMENTS : EXTRACTION INSTRUMENTS; Manufacturer: DEPUY ORTHOPAEDICS INC US.
| Device | ADAPTER REMOVER INSTRUMENT |
|---|---|
| Generic name | HIP INSTRUMENTS : EXTRACTION INSTRUMENTS |
| Manufacturer | DEPUY ORTHOPAEDICS INC US |
| Report number | 1818910-2020-11382 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | PRODUCT COMPLAINT # (B)(4). THIS REPORT IS BEING SUBMITTED PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803. THIS REPORT MAY BE BASED ON INFORMATION WHICH HAS NOT BEEN INVESTIGATED OR VERIFIED PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY DEPUY SYNTHES JOINT RECONSTRUCTION, OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE PRODUCT, DEPUY SYNTHES |
| Source | openFDA MAUDE (device adverse events) |
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