BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AC POWERCHARGER

    MDR report key: 377573 · Received February 13, 2002

    Report

    Report Number
    1220908-2002-00187
    Event Type
    Malfunction
    Date Received
    February 13, 2002
    Report Date
    January 16, 2002
    Manufacturer
    ZOLL MEDICAL CORP.
    Product Code
    KRF
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    COMPLAINANT ALLEGED THAT AFTER UNPLUGGING THE POWERCHARGER FROM THE WALL AC OUTLET, THE NURSE INADVERTENTLY TOUCHED THE AC PLUG'S METAL PRONGS AND REC'D AN ELECTRICAL SHOCK. THE COMPLAINANT INDICATED THAT THE NURSE WHO REC'D THE ELECTRICAL SHOCK DID NOT REQUIRE ANY MEDICAL ATTENTION AFTER THE EVENT OCCURRED, AND THE NURSE DID NOT SUFFER ANY LINGERING SIDE EFFECTS AS A RESULT OF THE SHOCK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AC POWERCHARGER AC POWER/BATTERY CHARGER KRF ZOLL MEDICAL CORP. 80400001 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other