BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PIP, INC.

    MDR report key: 222158 · Received May 5, 1999

    Report

    Report Number
    1062078-1999-00091
    Event Type
    Malfunction
    Date Received
    May 5, 1999
    Date of Event
    February 1, 1999
    Report Date
    April 22, 1999
    Manufacturer
    PIP, INC.
    Product Code
    FWM
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    RUPTURED IMPLANTS BILATERAL, REASON UNK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PIP, INC. Implant BREAST IMPLANT FWM PIP, INC. TEXTURED 96143

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Other