MODULAR ACETABULAR LINER Adverse Event — Injury (MDR 1825034-2008-00065)
MODULAR ACETABULAR LINER Adverse Event — Injury (MDR 1825034-2008-00065) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MODULAR ACETABULAR LINER; Manufacturer: BIOMET, INC.; Report number: 1825034-2008-00065.
| Device | MODULAR ACETABULAR LINER |
|---|---|
| Manufacturer | BIOMET, INC. |
| Report number | 1825034-2008-00065 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-20 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT PATIENT UNDERWENT REVISION TOTAL HIP ARTHROPLASTY IN 2002. SUBSEQUENTLY, THE PATIENT'S HIP DISLOCATED AND REVISION PROCEDURE WAS PERFORMED 2008. ACETABULAR LINER AND MODULAR HEAD COMPONENTS WERE REPLACED WITH A CONSTRAINED LINER AND MODULAR HEAD COMPONENT. |
| Source | openFDA MAUDE (device adverse events) |
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