UNKNOWN SHELL Adverse Event — Injury (MDR 3005751028-2020-00043)
UNKNOWN SHELL Adverse Event — Injury (MDR 3005751028-2020-00043) 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 | 3005751028-2020-00043 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, LITERATURE |
| Narrative | (B)(4). CONCOMITANT MEDICAL PRODUCT S: UNKNOWN ACETABULAR AUGMENT, UNKNOWN FEMORAL STEM, UNKNOWN FEMORAL HEAD, UNKNOWN ACETABULAR LINER. REPORT SOURCE - (B)(6). NO PRODUCT WAS RETURNED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. MEDICAL RECORDS WERE NOT PROVIDED. PART AND LOT IDENTIFICATION ARE NECESSARY FOR REVIEW OF DEVICE HISTORY RECORDS, NEITHER WERE PROVIDED. A DEFINITIVE ROOT |
| Source | openFDA MAUDE (device adverse events) |
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