BEUDAMED
    FDA Adverse Event Other Summary report: N

    PHILIPS

    MDR report key: 1141844 · Received August 27, 2008

    Report

    Report Number
    MW5008124
    Event Type
    Other
    Date Received
    August 27, 2008
    Date of Event
    August 17, 2008
    Report Date
    August 27, 2008
    Manufacturer
    PHILIPS
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    POSSIBLE PHILIPS MONITOR FAILURE IN A PRE-HOSPITAL SETTING. WE ARE UNABLE TO CONFIRM PROPER DEFIBRILLATION WHILE GIVING CARE TO PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PHILIPS PHILIPS HEARTSTART MRX LDD PHILIPS MRX *

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Other