BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ELEVATE APICAL AND POSTERIOR

    MDR report key: 2880831 · Received December 13, 2012

    Report

    Report Number
    2183959-2012-03248
    Event Type
    Injury
    Date Received
    December 13, 2012
    Report Date
    October 31, 2012
    Manufacturer
    AMERICAN MEDICAL SYSTEMS, INC.
    Product Code
    FTL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SHOULD ADD¿L INFO BECOME AVAILABLE REGARDING THIS EVENT IT WILL BE RE-EVALUATED AND A FOLLOW-UP REPORT WILL BE SENT. LAWYER-FILED REPORT - (B)(4).

    Description of Event or Problem · 1

    RELATED TO MFR #: 2183959-2012-03246 AND 2183959-2012-03247. IT WAS REPORTED BY THE PLAINTIFF'S ATTORNEY THAT THE PLAINTIFF EXPERIENCED EMOTIONAL DISTRESS AND A PROBLEM WITH THE PRODUCT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ELEVATE APICAL AND POSTERIOR SURGICAL MESH FTL AMERICAN MEDICAL SYSTEMS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Disability ELEVATE APICAL AND ANTERIOR| MINIARC PRECISE| MINIARC PRECISE| ELEVATE APICAL AND ANTERIOR