OXFORD PHASE III FEMORAL COMPONENT Adverse Event — Injury (MDR 1825034-2008-00063)
OXFORD PHASE III FEMORAL COMPONENT Adverse Event — Injury (MDR 1825034-2008-00063) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: OXFORD PHASE III FEMORAL COMPONENT; Manufacturer: BIOMET, INC.; Report number: 1825034-2008-00063.
| Device | OXFORD PHASE III FEMORAL COMPONENT |
|---|---|
| Manufacturer | BIOMET, INC. |
| Report number | 1825034-2008-00063 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-18 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT PATIENT UNDERWENT PARTICAL KNEE REPLACEMENT PROCEDURE IN 2003. SUBSEQUENTLY, RADIOGRAPHS INDICATE THAT ANTERIOR PORTION OF COMPONENT HAD FRACTURED. REVISION PROCEDURE WAS PERFORMED 2008. NO FURTHER DETAILS HAVE BEEN PROVIDED. |
| Source | openFDA MAUDE (device adverse events) |
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