BEUDAMED
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    ZOLL MEDICAL CORP

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·February 2, 2004

    ZOLL MEDICAL CORP

    FDA Adverse Event
    Malfunction ·ZOLL·Product code MLN·June 14, 2010

    ZOLL MEDICAL CORP.

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP.·Product code MKJ·April 9, 2009

    ZOLL MEDICAL CORP

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP·Product code MKJ·December 30, 2005

    ZOLL MEDICAL CORP

    FDA Adverse Event
    Injury ·ZOLL MEDICAL CORP·Product code MLN·March 23, 2000

    ZOLL MEDICAL CORP.

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP.·Product code LDD·February 11, 2000

    ZOLL MEDICAL CORP.

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 21, 2004

    ZOLL MEDICAL CORP

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP.·Product code LDD·February 10, 1997

    ZOLL MEDICAL CORP

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 2, 2005

    ZOLL MEDICAL CORP

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP.·Product code LDD·July 9, 1999

    ZOLL MEDICAL CORP

    FDA Adverse Event
    Injury ·ZOLL MEDICAL CORP·Product code MKJ·April 3, 2001

    ZOLL MEDICAL CORP.

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP.·Product code LDD·December 18, 1998

    ZOLL MEDICAL CORP

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 4, 2019

    Zoll Pediatric Electrodes labeled: Pedi Padz Multi-Function Electrode part Number: 8900-2065

    FDA Recall
    Terminated ·Bio-Detek, Inc.·Product code DRF·July 30, 2004

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 7, 2011

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 21, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 2, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 31, 2011

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 25, 2011

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 21, 2010