BEUDAMED
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    OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·August 6, 2015

    Oxy Serve II Oxygen Conserving Regulator, Model Number: MCRB-870-6, Superior Products, Inc/SP Medical, LLC, Cleveland, Ohio 44144

    FDA Recall
    Terminated ·Superior Products Inc·Product code NFB·October 19, 2007

    LGN PS HIGH FLEX XLPE SZ 7-8 11MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·June 2, 2019

    UNK_NAVISTAR RMT THERMOCOOL

    FDA Adverse Event
    Death ·BIOSENSE WEBSTER INC·Product code LPB·May 12, 2020

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code NVY·November 16, 2018

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·September 29, 2020

    TRANSVENE SVC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·September 4, 2020

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code NVY·May 1, 2018

    SPRINT

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·April 16, 2019

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·June 1, 2018

    SPRINT

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 8, 2017

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·February 26, 2020

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·December 17, 2014

    SPRINT QUATTRO SECURE MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVY·November 12, 2019

    VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 13, 2020

    ENDOTAK SQ

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code LWS·July 8, 2013

    SPRINT QUATTRO SECURE MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·November 8, 2022

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·March 20, 2020

    EVERA XT DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC EUROPE SARL·Product code LWS·December 20, 2018

    SUBCUTANEOUS, UNIPOLAR LEAD

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 24, 2020