BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK MESH

    MDR report key: 2964119 · Received February 8, 2013

    Report

    Report Number
    MW5028970
    Event Type
    Injury
    Date Received
    February 8, 2013
    Date of Event
    June 18, 2012
    Report Date
    February 8, 2013
    Manufacturer
    UNK
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    PHYSICIAN ASSISTANT

    Narratives

    Description of Event or Problem · 1

    URINARY RETENTION FROM PUBOVAGINAL SLING WHICH REQUIRED REMOVAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    55197 UNK MESH UNK MESH FTL UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Hospitalization