BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK PELVICOL PRODUCT

    MDR report key: 3191154 · Received June 21, 2013

    Report

    Report Number
    9617613-2013-00357
    Event Type
    Injury
    Date Received
    June 21, 2013
    Date of Event
    December 2, 2002
    Report Date
    May 28, 2013
    Manufacturer
    COVIDIEN
    Product Code
    FTL
    PMA / PMN Number
    K992556
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    PROCEDURE TYPE: UROGYNECOLOGICAL. ACCORDING TO THE REPORTER: THE PATIENT ALLEGED INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    283661 UNK PELVICOL PRODUCT PELVICOL MESH FTL COVIDIEN

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Other