BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN PELVICOL PRODUCT

    MDR report key: 3220986 · Received July 3, 2013

    Report

    Report Number
    9617613-2013-00469
    Event Type
    Injury
    Date Received
    July 3, 2013
    Date of Event
    February 11, 2005
    Report Date
    June 11, 2013
    Manufacturer
    COVIDIEN, FORMERLY TISUE
    Product Code
    FTL
    PMA / PMN Number
    K992556
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

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

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    305709 UNKNOWN PELVICOL PRODUCT PELVICOL MESH FTL COVIDIEN, FORMERLY TISUE

    Patients

    Seq Age Sex Outcome Treatment
    1 Female Other