AGC PATELLA BUTTON Adverse Event — Injury (MDR 3002806535-2008-00001)
AGC PATELLA BUTTON Adverse Event — Injury (MDR 3002806535-2008-00001) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AGC PATELLA BUTTON; Manufacturer: BIOMET UK LTD.; Report number: 3002806535-2008-00001.
| Device | AGC PATELLA BUTTON |
|---|---|
| Manufacturer | BIOMET UK LTD. |
| Report number | 3002806535-2008-00001 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Foreign, Company representation |
| Narrative | IT WAS REPORTED THAT PATIENT UNDERWENT KNEE PROCEDURE IN 2007. SUBSEQUENTLY, SEVEN MONTHS LATER, THE PATELLA COMPONENT BROKE OFF AND BECAME LOOSE IN THE KNEE. PATIENT WAS REVISED THE FOLLOWING MONTH. |
| Source | openFDA MAUDE (device adverse events) |
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