BEUDAMED
    FDA Adverse Event Summary report: N

    MICRO ABG KIT

    MDR report key: 202935 · Received December 18, 1998

    Report

    Report Number
    1718887-1998-00007
    Date Received
    December 18, 1998
    Date of Event
    November 12, 1998
    Report Date
    December 17, 1998
    Manufacturer
    MARQUEST MEDICAL PRODUCTS, INC.
    Product Code
    CBT
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    AFTER OBTAINING THE BLOOD SAMPLE THE NEEDLE WAS INSERTED INTO THE GEL FILLED SHEATH. AFTER APPLYING DIGITAL PRESSURE TO THE PUNCTURE SITE THE NEEDLE AND SHEATH WERE REMOVED AND REPLACED WITH LUER TIP CAP. WHILE ATTEMPTING TO PLACE THE GEL FILLED SHEATH IN THE SHARPS CONTAINER THE DEVICE WAS SOMEHOW DEFLECTED CAUSING IT TO FALL OFF. WHICH RESULTED IN THE CLINICIAN SUSTAINING A NEEDLE PRICK IN THE PALM OF THEIR HAND.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICRO ABG KIT ARTERIAL BLOOD GAS SAMPLER CBT MARQUEST MEDICAL PRODUCTS, INC. NA 111365

    Patients

    Seq Age Sex Outcome Treatment
    1 *