BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 446475 · Received March 4, 2003

    Report

    Report Number
    446475
    Event Type
    Other
    Date Received
    March 4, 2003
    Date of Event
    February 26, 2003
    Report Date
    March 3, 2003
    Manufacturer
    UNK
    Product Code
    HWC
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    SCREW X 2 REMOVED - S/P FX ANKLE - PAINFUL HARDWARE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK UNK HWC UNK UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR Other