BEUDAMED
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    PATHFINDER 700 HOLTER ANALYZER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ophthalmic Forceps

    FDA UDI
    KATENA PRODUCTS, INC.·00841668106204·HARMS-COLIBRI FORCEPS LONG

    NIO 2MP-21

    FDA 510(k)
    FDA Class 2 ·Radiology

    REDAPT¿ Revision Femoral System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLAIR ENDOVASCULAR STENT GRAFT

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code MIH·December 28, 2010

    CAPSUREFIXNOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 9, 2013

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE INC.·Product code LZG·July 7, 2014

    XSYSTEMS Dilution Buffer, list number 9519-02; for In Vitro diagnostic use, Bovine gamma globulin in Phosphate buffer, with Sodium Azide as a preservative; 950 mL bottle, 4 bottles per carton; Abbott Laboratories, Abbott Park, IL 60064 USA

    FDA Recall
    Terminated ·Abbott Laboratories HPD/ADD/GPRD·Product code JJE·September 1, 2004