BEUDAMED
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    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code LJS·April 3, 2026

    SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·December 22, 2021

    SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·July 1, 2017

    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code LJS·April 2, 2026

    Catheter, intravascular, therapeutic, short-term less than 30 days

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·November 10, 2022

    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code LJS·April 7, 2026

    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code LJS·March 2, 2026

    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code LJS·February 12, 2026

    BD PRECISIONGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·December 14, 2017

    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code LJS·February 12, 2026

    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code LJS·February 12, 2026

    ABBOCATH-T 20G 1-1/4

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code FOZ·April 27, 2009

    INSYTE AUTOGUARD PNK 20GA X 1.16IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 14, 2019

    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC·Product code LJS·October 21, 2025

    BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 25, 2019

    BD NEXIVA¿ SINGLE PORT WITH MAXZERO¿ CLOSED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·March 8, 2023

    ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER. Product Usage: Indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring cental venous access including, but not limited to: multiple infusions of fluids, medications, or chemotherapy, infusion of fluids that are hypertonic, hyperosmolar, or have divergent pH values, frequent blood sampling or blood/blood component infusions, infusion of incompatible medications, central venous pressure monitoring, lack of usable peripheral IV sites, replacement of multiple peripheral sites for IV access and injection of contrast media.

    FDA Enforcement
    Class II ·Terminated·Arrow International Inc·July 13, 2016

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 6, 2022

    BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 26, 2019

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·April 21, 2020