TAPERFILL HIP Adverse Event — Injury (MDR 1644408-2020-00358)
TAPERFILL HIP Adverse Event — Injury (MDR 1644408-2020-00358) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TAPERFILL HIP; Generic name: TAPERFILL HIP STEM, STANDARD, SIZE 15; Manufacturer: ENCORE MEDICAL L.P..
| Device | TAPERFILL HIP |
|---|---|
| Generic name | TAPERFILL HIP STEM, STANDARD, SIZE 15 |
| Manufacturer | ENCORE MEDICAL L.P. |
| Report number | 1644408-2020-00358 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | THE REASON FOR THIS REVISION SURGERY WAS REPORTED AS PERI-PROSTHETIC FRACTURE. THE PREVIOUS SURGERY AND THE SURGERY DETAILED IN THIS EVENT OCCURRED 1 DAY APART. THE HEALTHCARE PROFESSIONAL INDICATED THERE WAS NO DELAY IN SURGERY AND ANOTHER SUITABLE DEVICE WAS AVAILABLE FOR USE. THE REVISION SURGERY WAS COMPLETED AS INTENDED. THE DEVICES WERE DISPOSED OF AT HOSPITAL AND NOT MADE AVAILABLE TO DJO S |
| Source | openFDA MAUDE (device adverse events) |
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