BEUDAMED
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    ST. JUDE MEDICAL INC.

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code DRF·January 3, 2012

    ST JUDE MEDICAL, INC

    FDA Adverse Event
    Death ·ST JUDE MEDICAL, INC·Product code FZP·August 16, 2002

    ST JUDE MEDICAL, INC

    FDA Adverse Event
    Death ·ST JUDE MEDICAL, INC.·Product code LWQ·September 8, 1994

    ST JUDE MEDICAL INC.

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC.·Product code LWS·May 23, 2007

    ST. JUDE MEDICAL INC.

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL, INC.·Product code LWQ·February 24, 1998

    ST JUDE MEDICAL INC

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC·Product code DTB·July 10, 2006

    GALLANT DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC. (AFD CAT-SUNNYVALE)·Product code NIK·February 21, 2025

    RIATA ACTIVE-FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 30, 2006

    GALLANT VR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·May 15, 2025

    TVL-ADX ACTIVE-FIXATION STEROID-ELUTING TACHYARRHYTHMIA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 8, 2006

    ST. JUDE MEDICAL INC., TEMPORARY PACEMAKER

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code LDF·July 19, 2016

    RIATA ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 27, 2006

    TVL-ADX ACTIVE-FIXATION STEROID-ELUTING TACHYARRHYTHMIA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 9, 2006

    ATLAS VR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CMRD·Product code LWS·July 14, 2006

    ATLAS + DR DUAL-CHAMBER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.CRMD·Product code LWS·June 27, 2006

    GALLANT DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·January 17, 2025

    GALLANT HF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC. (AFD CAT-SUNNYVALE)·Product code NIK·March 25, 2025

    RIATA ACTIVE-FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 7, 2006

    RIATA ACTIVE-FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 30, 2006

    PHOTON DR DUAL-CHAMBER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 8, 2006