BEUDAMED
    160 results · 16ms · Sources: EU EUDAMED, US FDA

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    Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·October 17, 2017

    Central Venous Catheterization Kit with Blue FlexTip Catheter; Product code: AK-04301; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·October 17, 2017

    Arrow Multi Lumen CVC Kit (Central venous catheter); Product Code: CDC-15703-1A; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·October 17, 2017

    ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter); Product Code: AK-45703-ACDC; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·October 17, 2017

    AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·October 17, 2017

    Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·October 17, 2017

    Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product code: ASK-45703-PHF2; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·October 17, 2017

    Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code: ASK 15703 NYP; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·October 17, 2017

    Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code: ASK-15703-PRWJ; Exp. Dates Feb 2018- Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·October 17, 2017

    Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous Catheterization Kit; Product Codes: ASK-45703-PNHS; ASK-45703-PGMCL; ASK-45703-PNW; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·October 17, 2017

    Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features, and Maximal Barrier Precautions Features; Product Code: ASK-12703-WMC1; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·October 17, 2017

    IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill syringes from 0.5mL up to 11.5mL using mixing instructions from its formulary to fill the orders.

    FDA Recall
    Terminated ·Baxter Healthcare Corp.·Product code NEP·November 8, 2013

    ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes: AK-22142-CDC, AK-22142-F, AK-25142-CDC, AK-25142-F; Exp. Dates Feb 2018 - Nov 2018

    FDA Recall
    Terminated ·Arrow International Inc·Product code MPB·October 17, 2017

    ECMO Reinforced Dual Lumen Cannula, 28Fr., REF: VV28F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.

    FDA Recall
    Terminated ·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018

    Reinforced Dual Lumen Cannula, 19Fr., REF: VV19F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.

    FDA Recall
    Terminated ·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018

    Reinforced Dual Lumen Cannula, 23Fr., REF: VV23F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.

    FDA Recall
    Terminated ·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018

    Reinforced Dual Lumen Cannula, 32Fr., REF: VV32F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.

    FDA Recall
    Terminated ·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018

    Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.

    FDA Recall
    Terminated ·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018

    Reinforced Dual Lumen Cannula, 16Fr., REF: VV16F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.

    FDA Recall
    Terminated ·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018

    AMS DURA-II Universal Tips, 2cm, Product Number 72009361, Sterile, American Medical Systems, Inc. Minnetonka, MN

    FDA Recall
    Terminated ·American Medical Systems·Product code FAE·February 19, 2007