BEUDAMED
    FDA Adverse Event Other Summary report: N

    VANISHPOINT

    MDR report key: 1040898 · Received May 9, 2008

    Report

    Report Number
    MW5006816
    Event Type
    Other
    Date Received
    May 9, 2008
    Date of Event
    May 5, 2008
    Report Date
    May 6, 2008
    Manufacturer
    RETRACTABLE TECHNOLOGIES
    Product Code
    FMF
    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 1ML 27G X 1/2" FMF RETRACTABLE TECHNOLOGIES G060610

    Patients

    Seq Age Sex Outcome Treatment
    1