BEUDAMED
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    SEMINAL FLUID COLLECTION KIT II

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LEXINGTON MEM W COLUMBIA SC 2

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·October 30, 2013

    BIO-FIT HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GISH ARTERIAL FILTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROTECTA VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 11, 2013

    PROMOTE PLUS CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·January 10, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 24, 2014

    Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.

    FDA Recall
    Terminated ·Clinical Diagnostic Solutions·Product code JPK·March 24, 2011

    Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.

    FDA Recall
    Terminated ·Clinical Diagnostic Solutions·Product code JPK·March 24, 2011

    Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.

    FDA Recall
    Terminated ·Clinical Diagnostic Solutions·Product code JPK·March 24, 2011