BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUIK ABG KIT

    MDR report key: 158846 · Received March 17, 1998

    Report

    Report Number
    1718887-1998-00001
    Event Type
    Malfunction
    Date Received
    March 17, 1998
    Report Date
    March 17, 1998
    Manufacturer
    MARQUEST MEDICAL PRODUCTS, INC.
    Product Code
    CBT
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Narratives

    Description of Event or Problem · 1

    THE AMOUNT OF GEL IN THE NEEDLE SHEATH IS NOT SUFFICIENT TO KEEP NEEDLE IN THE SHEATH. WHILE THE CLINICIAN WAS AGITATING THE SYRINGE THE GEL FILLED SHEATH CAME OFF. THE CLINICIAN STUCK THEMSELF WITH A CONTAMINATED NEEDLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUIK ABG KIT ARTERIAL BLOOD GAS SAMPLING SYRINGE CBT MARQUEST MEDICAL PRODUCTS, INC. NA 108451

    Patients

    Seq Age Sex Outcome Treatment
    1 *