UNKNOWN ACETABULAR SHELL Adverse Event — Injury (MDR 3005751028-2020-00037)
UNKNOWN ACETABULAR SHELL Adverse Event — Injury (MDR 3005751028-2020-00037) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN ACETABULAR SHELL; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER TMT.
| Device | UNKNOWN ACETABULAR SHELL |
|---|---|
| Generic name | PROSTHESIS, HIP |
| Manufacturer | ZIMMER TMT |
| Report number | 3005751028-2020-00037 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | LITERATURE |
| Narrative | (B)(4). CONCOMITANT MEDICAL PRODUCT: UNKNOWN FEMORAL HEAD; UNKNOWN ACETABULAR LINER; UNKNOWN SCREW; UNKNOWN FEMORAL STEM. 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 BE |
| Source | openFDA MAUDE (device adverse events) |
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