UNKNOWN SHELL Adverse Event — Injury (MDR 3005751028-2020-00040)
UNKNOWN SHELL Adverse Event — Injury (MDR 3005751028-2020-00040) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN SHELL; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER TMT.
| Device | UNKNOWN SHELL |
|---|---|
| Generic name | PROSTHESIS, HIP |
| Manufacturer | ZIMMER TMT |
| Report number | 3005751028-2020-00040 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | FOREIGN |
| Narrative | (B)(4). CONCOMITANT MEDICAL PRODUCTS: UNKNOWN FEMORAL HEAD, UNKNOWN ACETABULAR LINER, UNKNOWN FEMORAL STEM, UNKNOWN SCREW. REPORT SOURCE, LITERATURE - WEBB, J.E. ET AL (2017). THE DOUBLE-CUP CONSTRUCT: A NOVEL TREATMENT STRATEGY FOR THE MANAGEMENT OF PAPROSKY IIIA AND IIIB ACETABULAR DEFECTS. THE JOURNAL OF ARTHROPLASTY, 32(9), 25-31. DOI: 10.1016/J.ARTH.2017.04.017. REPORTED EVENT WAS UNABLE TO B |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →