BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIOPINCE ANGIOTECH

    MDR report key: 1061345 · Received June 16, 2008

    Report

    Report Number
    MW5007315
    Event Type
    Malfunction
    Date Received
    June 16, 2008
    Date of Event
    June 12, 2008
    Report Date
    June 16, 2008
    Product Code
    KNW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ANGIO TECH PRODUCT 18 X 10 BIOPSY NEEDLE LOT # 80491LIC 2 NEEDLES DID NOT "COCK" PROPERLY IN ORDER TO PERFORM THE BIOPSY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOPINCE ANGIOTECH NONE KNW 80491LIC

    Patients

    Seq Age Sex Outcome Treatment
    1 17 YR