BEUDAMED
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    RAAF DUAL LUMEN CATH. REPAIR KIT 2.2

    FDA 510(k)
    FDA Class 2 ·General Hospital

    THE TOOTHPIK

    FDA 510(k)
    FDA Class 1 ·Dental

    GAS-STAT MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 28, 2014

    SECURA DR

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LWS·November 15, 2012

    ASTRAL 150 DBL KIT FRA

    FDA Adverse Event
    Malfunction ·RESMED LTD.·Product code NOU·June 3, 2015

    MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·October 18, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018