BEUDAMED
    FDA Adverse Event Summary report: N

    DEPUY

    MDR report key: 2152612 · Received January 24, 2011

    Report

    Report Number
    2152612
    Date Received
    January 24, 2011
    Report Date
    January 24, 2011
    Product Code
    JDI
    Report Source
    User Facility report
    Reporter Location
    VA, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    HAVE HAD 3 DEPUY HIP EXPLANTS OVER THE LAST MONTH AND A HALF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DEPUY DEPUY HIP REPLACEMENT JDI * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *