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    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·June 13, 2018

    ZM-530PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code DRT·May 22, 2018

    R SERIES PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·April 6, 2018

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·May 31, 2018

    ZM-531PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code DRT·June 12, 2018

    ZM-530PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code DRT·May 3, 2018

    GZ-120PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code DRT·April 17, 2018

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·April 5, 2018

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·April 4, 2018

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·June 13, 2018

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·June 21, 2016

    ZM-541PA

    FDA Adverse Event
    Other ·NIHON KOHDEN TOMIOKA CORPORATION·Product code DRT·May 13, 2016

    ZM-530PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN TOMIOKA CORPORATION·Product code DRT·June 3, 2016

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·May 24, 2016

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·May 22, 2017

    ZM-530PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code DRT·May 8, 2017

    ZM-521PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code DRT·April 24, 2017

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·May 15, 2017

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DRT·May 2, 2017

    ZM-530PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code DRT·February 12, 2020