MODULAR HEAD/COCR Adverse Event — Injury (MDR 1825034-2008-00018)
MODULAR HEAD/COCR Adverse Event — Injury (MDR 1825034-2008-00018) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MODULAR HEAD/COCR; Generic name: JDI; Manufacturer: BIOMET, INC..
| Device | MODULAR HEAD/COCR |
|---|---|
| Generic name | JDI |
| Manufacturer | BIOMET, INC. |
| Report number | 1825034-2008-00018 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-01-18 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT PT UNDERWENT BI-POLAR HIP PROCEDURE IN 2007. SUBSEQUENTLY, MODULAR HEAD COMPONENT DISASSOCIATED AND LOOSENING OF THE STEM COMPONENT WAS NOTED DURING REVISION PROCEDURE ON ABOUT 15 DAYS LATER. |
| Source | openFDA MAUDE (device adverse events) |
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