BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CARDINAL HEALTH BATTERY

    MDR report key: 2511286 · Received March 23, 2012

    Report

    Report Number
    MW5024814
    Event Type
    Injury
    Date Received
    March 23, 2012
    Date of Event
    March 22, 2012
    Report Date
    March 23, 2012
    Manufacturer
    CARDINAL HEALTH
    Product Code
    DSZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A 9V BATTERY POWERING TEMPORARY PACEMAKER FAILED. PT WAS PACEMAKER DEPENDENT AND HAD CARDIAC STANDSTILL. EVENT REAPPEARED AFTER REINTRODUCTION: YES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CARDINAL HEALTH BATTERY 9V BATTERY DSZ CARDINAL HEALTH 9V 110223-SH

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Life Threatening