BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PREMIUM SURGICLIP II M-11.5 TITANIUM

    MDR report key: 3042012 · Received April 2, 2013

    Report

    Report Number
    2647580-2013-00173
    Event Type
    Injury
    Date Received
    April 2, 2013
    Report Date
    March 8, 2013
    Manufacturer
    COVIDIEN, FORMERLY USSC PUERTO RICO
    Product Code
    FZP
    PMA / PMN Number
    K853650
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    ACCORDING TO THE REPORTER: THE LAST CLIP CUT THE VEIN ON WHICH IT WAS SUPPOSED TO BE PUT ON. THERE WAS UNEXPECTED BLEEDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    134223 PREMIUM SURGICLIP II M-11.5 TITANIUM DISPOSABLE CLIP APPLIER FZP COVIDIEN, FORMERLY USSC PUERTO RICO P2H0115X

    Patients

    Seq Age Sex Outcome Treatment
    1 Other