BEUDAMED
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    ON-Q BY I-FLOW

    FDA Adverse Event
    Injury ·I FLOW·Product code BSO·January 13, 2010

    ON-Q-SOAKER 6.5 DUEL SITE PAIN MGM SYSTEM

    FDA Adverse Event
    Injury ·I-FLOW·Product code LKK·May 14, 2001

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·February 23, 2016

    HOME PUMP/ECLIPSE

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·September 13, 2005

    HOMEPUMP ECLIPSE 250ML, 175ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW CORP.·Product code MEB·January 21, 2011

    MW5055987

    FDA Adverse Event
    Injury ·September 1, 2015

    ECLIPSE HOMEPUMP

    FDA Adverse Event
    Malfunction ·I-FLOW CORP·Product code MEB·May 1, 2007

    HOMEPUMP BY I-FLOW MODEL (060020-A)

    FDA Adverse Event
    Malfunction ·I-FLOW CORP.·Product code MEB·June 24, 1998

    EGIA 60 ARTICULATING MED/THICK SULU

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·June 23, 2015

    ESSURE

    FDA Adverse Event
    Injury ·BAYER HEALTHCARE LLC·Product code HHS·August 8, 2018

    EGIA 60 ARTICULATING MED/THICK SULU

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·June 26, 2015

    FILSHIE CLIPS

    FDA Adverse Event
    Injury ·COOPER SURGICAL·Product code KNH·February 24, 2017

    ICY HOT HEAT THERAPY

    FDA Adverse Event
    Injury ·CHATTEM, INC·Product code IMD·February 12, 2008

    ON-Q PAINBUSTER

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·June 2, 2005

    HOMEPUMP C-SERIES

    FDA Adverse Event
    Malfunction ·KIMBERLY CLARK·Product code MEB·July 1, 2015

    ON-Q C-BLOC WITH ONDEMAND

    FDA Adverse Event
    Malfunction ·I-FLOW CORPORATION·Product code MEB·March 27, 2007

    ASPIRE SR MODEL 106 GENERATOR

    FDA Adverse Event
    Injury ·CYBERONICS, INC. / LIVANOVA USA, INC·Product code MUZ·October 4, 2023

    ESSURE

    FDA Adverse Event
    Injury ·BAYER HEALTHCARE, LLC·Product code HHS·September 20, 2018

    TECNIS OPTIBLUE ITEC PRELOADED 1-PIECE IOL

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL OPTICS·Product code HQL·September 1, 2017

    KETOSENS BLOOD BETA-KETONE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·I-SENS, INC.·Product code JIN·January 26, 2022