BEUDAMED
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    THERASEED IN MICK CARTRIDGES, STERILE

    FDA Adverse Event
    Malfunction ·BARD BRACHYTHERAPY, INC. -1424526·Product code KXK·December 6, 2016

    I125 SEEDS IN QUICKLINK CARTRIDGE (IN PEWTER TRAY), STERILE, CE MARKED

    FDA Adverse Event
    Malfunction ·BARD BRACHYTHERAPY, INC. -1424526·Product code KXK·December 30, 2016

    PD103 SEEDS LOADED IN MICK CARTRIDGES, STERILE

    FDA Adverse Event
    Malfunction ·BARD BRACHYTHERAPY, INC. -1424526·Product code KXK·November 16, 2016

    IODINE (I-125) SEEDS

    FDA Adverse Event
    Injury ·GE HEALTHCARE·Product code KXK·March 6, 2009

    BRACHYSOURCE IODINE - 125 SEEDS IN MICK CARTRIDGE

    FDA Adverse Event
    Malfunction ·BARD BRACHYTHERAPY, INC.·Product code KXK·June 20, 2014

    THERASHERE, YTTRIUM-90 GLASS MICROSPHERES

    FDA Adverse Event
    Product code KXK·June 3, 2014

    SIR-SPHERES

    FDA Adverse Event
    SIRTEX MEDICAL LIMITED·Product code KXK·February 18, 2004

    RAPIDSTRAND RX

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code KXK·July 29, 2015

    MAMMOSITE RTS

    FDA Adverse Event
    Injury ·PROXIMA THERAPEUTICS, INC.·Product code KXK·January 29, 2004

    GLIASITE RADIATION THERAPY SYSTEM

    FDA Adverse Event
    Injury ·PROXIMA THERAPEUTICS·Product code KXK·February 6, 2004

    GLIASITE RADIATION THERAPY SYSTEM

    FDA Adverse Event
    Injury ·PROXIMA THERAPEUTICS, INC.·Product code KXK·January 12, 2004

    SIR-SPHERES

    FDA Adverse Event
    SIRTEX MEDICAL LIMITED·Product code KXK·January 20, 2004

    GLIASITE RADIATION THERAPY SYSTEM

    FDA Adverse Event
    Injury ·PROXIMA THERAPEUTICS, INC.·Product code KXK·February 19, 2004

    GLIASITE RADIATION THERAPY SYSTEM (RTS)

    FDA Adverse Event
    Injury ·PROXIMA THERAPEUTICS, INC.·Product code KXK·March 3, 2004

    BARD® QUICKLINK¿ CARTRIDGES WITH BRACHYSOURCE® I-125 SEEDS

    FDA Adverse Event
    Malfunction ·BARD BRACHYTHERAPY, INC. -1424526·Product code KXK·December 29, 2017

    I125 SEEDS IN QUICKLINK, STERILE, 13.1 MBQ

    FDA Adverse Event
    Malfunction ·Product code KXK·June 29, 2021

    0.50MCI 1251 BRACHYSOURCE

    FDA Adverse Event
    Malfunction ·BARD BRACHYTHERAPY, INC. -1424526·Product code KXK·May 20, 2021

    IODINE (I-125) SEEDS IN CARRIER

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code KXK·December 29, 2014

    BARD® BRACHYSOURCE® I-125 IMPLANT SEED

    FDA Adverse Event
    Malfunction ·BARD BRACHYTHERAPY, INC. -1424526·Product code KXK·November 21, 2017

    BARD® QUICKLINK¿ CARTRIDGES WITH BRACHYSOURCE® I-125 SEEDS

    FDA Adverse Event
    Malfunction ·BARD BRACHYTHERAPY, INC. -1424526·Product code KXK·November 17, 2017