TRABECULAR METAL¿¢ ACETABULAR REVISION SHELL Adverse Event — Injury (MDR 3005751028-2020-00035)
TRABECULAR METAL¿¢ ACETABULAR REVISION SHELL Adverse Event — Injury (MDR 3005751028-2020-00035) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRABECULAR METAL¿¢ ACETABULAR REVISION SHELL; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER TMT.
| Device | TRABECULAR METAL¿¢ ACETABULAR REVISION SHELL |
|---|---|
| Generic name | PROSTHESIS, HIP |
| Manufacturer | ZIMMER TMT |
| Report number | 3005751028-2020-00035 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | CONSUMER, HEALTH PROFESSIONAL |
| Narrative | (B)(4). NO CLINICAL RECORDS, IMAGES, OR DEVICES WERE RETURNED FOR REVIEW. THE PATIENT¿S MEDICAL CONDITION CAN LEAD TO PAIN IN THE JOINTS DUE TO EASY BRUISING AND HYPEREXTENSION. AS NO ADDITIONAL RECORDS HAVE BEEN PROVIDED, THE DIAGNOSIS ALONE CANNOT RULE OUT THE DEVICE AS THE CAUSE OF THE PAIN IN THIS PATIENT AND DOES NOT ACCOUNT FOR THE ADDITIONAL ALLEGATIONS. A REVIEW OF THE DEVICE HISTORY RECOR |
| Source | openFDA MAUDE (device adverse events) |
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