BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 2903713 · Received December 29, 2012

    Report

    Report Number
    MW5028441
    Event Type
    Injury
    Date Received
    December 29, 2012
    Date of Event
    April 17, 2012
    Report Date
    December 29, 2012
    Manufacturer
    UNK
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AR, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    A SUTURE AND MESH FIBERS FOUND INSIDE BLADDER. REMOVAL (B)(6) 2012.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK MESH FOR HERNIA FTL UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Hospitalization| R