BEUDAMED
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    FDA Adverse Event
    Injury ·LAKE REGION MEDICAL LIMITED·Product code DQX·April 10, 2024

    QUADRA ASSURA MP ICD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·April 26, 2016

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 12, 2012

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTM·December 21, 2007

    CURRENT+ DR DUAL-CHMBR W/SJ4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·November 21, 2016

    UNIFY CRT-D, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·May 6, 2014

    CD2257-40Q FORTIFY ASSURA DR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·September 13, 2016

    ELLIPSE DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·October 11, 2018

    HYDRO-PRO brand Suction-Irrigation System without Probe, Disposable (single use only), sterile, latex free. R-Med Re-Order # 55170R; Distributed by R-Med, Inc., Orgeon, OH

    FDA Recall
    Terminated ·Vital Concepts, Inc.·Product code GCY·July 11, 2003

    FORTIFY ASSURA VR ICD, US

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·March 2, 2026

    SINGLE DISP TRANSPAC IV TRANSDUCER

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code BYR·December 23, 2003

    SINGLE DISP TRANSPAC IV TRANSDUCER

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code BYR·November 8, 2001

    2137

    FDA Adverse Event
    Other ·RICHARD WOLF MEDICAL INSTRUMENTS CORP·Product code FEO·September 6, 2005

    CONFIRM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code MXC·February 23, 2021

    CONFIRM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code MXC·October 15, 2019

    9611451-2007-00339

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·September 22, 2007

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE, LLC·Product code NDN·February 26, 2010

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012

    MECTALIF ANTERIOR ALIF TRIAL FLUSH - 35X27 - H.12 - L.10°

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·December 28, 2017

    CONFIRM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code MXC·January 17, 2019