TRABECULAR METAL ACETABULAR REVISION SYSTEM ACETABULAR AUGMENT Adverse Event — Injury (MDR 3005751028-2020-00059)
TRABECULAR METAL ACETABULAR REVISION SYSTEM ACETABULAR AUGMENT Adverse Event — Injury (MDR 3005751028-2020-00059) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRABECULAR METAL ACETABULAR REVISION SYSTEM ACETABULAR AUGMENT; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER T
| Device | TRABECULAR METAL ACETABULAR REVISION SYSTEM ACETABULAR AUGMENT |
|---|---|
| Generic name | PROSTHESIS, HIP |
| Manufacturer | ZIMMER TMT |
| Report number | 3005751028-2020-00059 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER, HEALTH PROFESSIONAL |
| Narrative | (B)(4). MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 3005751028 - 2020 - 00058. CONCOMITANT MEDICAL PRODUCT(S): UNK LINER; UNK STEM; STRYKER RESTORATION CUP 56 MM PART#1235-2-562 LOT#G5830067; STRYKER X3 SIZE 28/56 INSERT PART#1236-2-856 LOT#306413; CER OPTION TYPE 1 TPR SLEVE +6 PE 1 PART#650-1068 LOT#646880; DELTA CERAMIC OPTION HEAD DIA2 8 PART#650-1055 LOT#195 |
| Source | openFDA MAUDE (device adverse events) |
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