BEUDAMED
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    CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Injury ·NEOSTAR MEDICAL TECHNOLOGIES, INC.·Product code DQO·July 5, 1996

    NEO-STAR PHORESIS CATHETER

    FDA Adverse Event
    Injury ·NEOSTAR MEDICAL TECHNOLOGIES, INC.·Product code DQO·January 2, 1997

    AKCESS CATH-KIT

    FDA Adverse Event
    Death ·NEOSTAR MEDICAL TECHNOLOGIES, INC.·Product code BSY·August 16, 1993

    AKCESS CATH-KIT

    FDA Adverse Event
    Death ·NEOSTAR MEDICAL TECHNOLOGIES, INC.·August 16, 1993

    SUBCLAVIAN CATHETER

    FDA Adverse Event
    Malfunction ·NEOSTAR MEDICAL TECHNOLOGIES, INC.·Product code LFJ·September 8, 1995

    CIRCLE C SILICONE CATHETER KIT

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·September 28, 2000

    PHERES-FLOW CENTRAL VENOUS CATHETER KIT

    FDA Adverse Event
    Injury ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·September 28, 2000

    CIRCLE C SILICONE CATHETER KIT

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·August 23, 2000

    CIRCLE C SILICONE CATHETER KIT

    FDA Adverse Event
    Malfunction ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·July 14, 2000

    PHERES-FLOW CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Injury ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·April 6, 2000

    PHERES-FLOW CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Injury ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·April 6, 2000

    CENTRAL VENOUS CATHETER KIT

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·April 25, 2000

    INSERTION TRAY

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code KOC·June 13, 2000

    PHERES-FLOW CENTRAL VENOUS CATHETER KIT

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·June 8, 2000

    PHERES-FLOW CENTRAL VENOUS CATHETER KIT

    FDA Adverse Event
    Malfunction ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·April 5, 2000

    CIRCLE C SILICONE CATHETER KIT

    FDA Adverse Event
    Injury ·NEOSTAR MEDICAL TECHNOLOGIES/ HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·May 9, 2000

    CIRCLE C SILICONE CATHETER KIT

    FDA Adverse Event
    Injury ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·June 22, 2000

    INSERTION TRAY

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code KOC·April 12, 2000

    PHERES-FLOW CENTRAL VENOUS CATHETER KIT

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·May 3, 2000

    COILED PERITONEAL CATHETER

    FDA Adverse Event
    Injury ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·May 18, 1999