BEUDAMED
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    V SERIES MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·January 29, 2013

    IMPULSE GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQO·August 5, 2014

    SARNS CENTRIFUGAL PUMP

    FDA Adverse Event
    Injury ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·February 2, 2011