BEUDAMED
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    STENT - VASCULAR RECONSTRUCTION

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code NJE·January 8, 2019

    Cordis Neurovascular Pre-Shaped PROWLER Infusion Catheters.

    FDA Recall
    Terminated ·Cordis Neurovascular, Inc.·Product code KRA·August 11, 2006

    Cordis Neurovascular Pre-Shaped Prowler Select Infusion Catheters.

    FDA Recall
    Terminated ·Cordis Neurovascular, Inc.·Product code KRA·August 11, 2006

    Product is labeled as Cordis Pre-shaped Prowler Plus MP Infusion Catheter (3 F proximal OD, 2.3 F Distal OD, 45 cm distal length, total length 155 cm) with an MP (45 degree) dual marker band tip. Also the package states that it is distributed by Cordis Endovascular systems, Inc, Miami, FL 33102 a Johnson & Johnson Company.

    FDA Recall
    Terminated ·Cordis Neurovascular, Inc.·October 19, 2001

    PROWLER SELECT MICROCATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code KRA·March 21, 2012

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·March 20, 2012

    TRUFILL DCS ORBIT MINI COMPLEX FILL

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code HCG·January 20, 2012

    PROWLER SELECT MICROCATHETERS

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code KRA·February 1, 2012

    TRUFILL DCS ORBIT MINI COMPLEX FILL

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code HCG·January 20, 2012

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Death ·CORDIS NEUROVASCULAR, INC.·Product code NJE·February 6, 2012

    TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code HCG·March 22, 2012

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·January 8, 2012

    TRUFILL DCS ORBIT MINI COMPLEX FILL

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code HCG·February 7, 2012

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·February 23, 2012

    TRUFILL DCS ORBIT MINI COMPLEX FILL

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code HCG·January 17, 2012

    TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code HCG·February 7, 2012

    PROWLER MICROCATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code KRA·February 24, 2012

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code NJE·February 14, 2012

    PROWLER SELECT MICROCATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code KRA·March 16, 2012

    TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code HCG·March 21, 2012