BEUDAMED
    FDA Adverse Event Death Summary report: N

    LIFEPAK 15 CARDIAC MONITO

    MDR report key: 19467597 · Received June 4, 2024

    Report

    Report Number
    MW5155722
    Event Type
    Death
    Date Received
    June 4, 2024
    Date of Event
    May 25, 2024
    Report Date
    May 31, 2024
    Manufacturer
    STRYKER / PHYSIO-CONTROL, INC.
    Product Code
    MKJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    501
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PHYSICO CONTROL LIFEPAK 15 CARDIAC MONITOR FAILED TO TURN ON WHEN PLACED ON A CARDIAC ARREST PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    823490 LIFEPAK 15 CARDIAC MONITO AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE) MKJ STRYKER / PHYSIO-CONTROL, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR Female Death