BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PD1200 DEFIBRILLATOR/PACEMAKER

    MDR report key: 1181890 · Received September 25, 2008

    Report

    Report Number
    1220908-2008-02270
    Event Type
    Malfunction
    Date Received
    September 25, 2008
    Report Date
    September 17, 2008
    Manufacturer
    ZOLL MEDICAL CORPORATION
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ZOLL MEDICAL CORP HAS NOT RECEIVED THE DEVICE FOR EVAL, AND THIS COMPLAINT IS STILL UNDER INVESTIGATION.

    Description of Event or Problem · 1

    COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE INAPPROPRIATELY SHUT DOWN. COMPLAINANT INDICATED THAT THERE WAS NO PT INVOLVEMENT IN THE REPORTED MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PD1200 DEFIBRILLATOR/PACEMAKER DEFIBRILLATOR LDD ZOLL MEDICAL CORPORATION PD1200 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA