BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SWANSON SILASTIC IMPLANT

    MDR report key: 53125 · Received July 31, 1996

    Report

    Report Number
    53125
    Event Type
    Injury
    Date Received
    July 31, 1996
    Date of Event
    May 14, 1996
    Report Date
    May 21, 1996
    Manufacturer
    DOW CORNING CORP.
    Product Code
    KWF
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    FRACTURE OF IMPLANT OF LEFT LONG FINGER. DISLOCATION LEFT LONG FINGER MP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SWANSON SILASTIC IMPLANT Implant * KWF DOW CORNING CORP. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 60 YR Hospitalization