BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VANISHPOINT

    MDR report key: 1040899 · Received May 9, 2008

    Report

    Report Number
    MW5006817
    Event Type
    Malfunction
    Date Received
    May 9, 2008
    Date of Event
    May 5, 2008
    Report Date
    May 6, 2008
    Manufacturer
    RETRACTABLE TECHNOLOGIES
    Product Code
    RET
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    THE NEEDLE WOULD NOT RETRACT AFTER USE (UPON ACTIVATION).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VANISHPOINT TUBERCULIN SYRINGE 1 ML 27 G X 1/2" RET RETRACTABLE TECHNOLOGIES G061104

    Patients

    Seq Age Sex Outcome Treatment
    1