BEUDAMED
    FDA Adverse Event Other Summary report: N

    VANISHPOINT TUBERCULIN SYRINGE 1 CC

    MDR report key: 1027700 · Received April 9, 2008

    Report

    Report Number
    MW5006199
    Event Type
    Other
    Date Received
    April 9, 2008
    Report Date
    April 9, 2008
    Manufacturer
    RETRACTABLE TECHNOLOGIES, INC.
    Product Code
    FMF
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    TWO VANISHPOINT TUBERCULIN SYRINGES WERE REMOVED FROM SEALED PACKAGES, AND DID NOT CONTAIN NEEDLES. ONE VANISHPOINT 3CC SYRINGE WAS REMOVED FROM SEALED PACKAGE AND DID NOT CONTAIN A NEEDLE. DIAGNOSIS OR REASON FOR USE: #1 TB TESTING. #2 IM ADMINISTRATION OF MEDICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VANISHPOINT TUBERCULIN SYRINGE 1 CC NONE FMF RETRACTABLE TECHNOLOGIES, INC. G130A
    2 VANISHPOINT SYRINGE 3CC 21G X 1 1/2" NONE FMF RECTRACABLE TECHNOLOGIS, INC. A070403

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR