BEUDAMED
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    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·September 14, 2017

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·July 4, 2017

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·April 4, 2017

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·June 30, 2017

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·November 6, 2017

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·December 9, 2016

    ALINITY HQ PROCESSING MODULE

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code GKZ·October 18, 2023

    THERMAGE FLX (TG-3A) SYSTEM AND ACCESSORIES

    FDA Adverse Event
    Injury ·SOLTA MEDICAL INC.·Product code GEI·February 17, 2022

    SYNERGETICS 23 G DIRECTIONAL LASER PROBE

    FDA Adverse Event
    Malfunction ·SYNERGETICS·Product code HQB·February 26, 2012

    OPHTHALAS 532 LASER

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC.·Product code HQB·September 4, 1996

    25GA FLEXIBLE TAPERED ILLUMINATED LASER PROBE

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQB·June 15, 2022

    OPHTHALAS 532 EYELITE

    FDA Adverse Event
    Malfunction ·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQB·November 20, 2003

    ELITE E85

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code HQB·December 18, 2003

    OPHTHALAS 532 EYELITE

    FDA Adverse Event
    Injury ·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQB·December 24, 2003

    OPHTHALAS SP

    FDA Adverse Event
    Malfunction ·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQB·August 18, 2000

    25 GA CURVED LASER PROBE

    FDA Adverse Event
    Injury ·PEREGRINE SURGICAL LLC·Product code HQB·November 7, 2025

    ALCON SHIELDED BULLET ILLUMINATOR

    FDA Adverse Event
    Injury ·ALCON SURGICAL·Product code HQB·March 27, 2013

    ALCON

    FDA Adverse Event
    Injury ·ALCON SURGICAL·Product code HQB·February 18, 2013

    OERTLI SWITZERLAND

    FDA Adverse Event
    Injury ·VORTEX SURGICAL INC.·Product code HQB·December 2, 2025

    NOVUS 2000

    FDA Adverse Event
    Injury ·LUMENIS, INC. (FORMERLY COHERENT)·Product code HQB·April 5, 2005