BEUDAMED
    15 results · 64ms · Sources: EU EUDAMED, US FDA

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    COVIDIEN LIGASURE

    FDA Adverse Event
    Injury ·MEDTRONIC/ FORMERLY COVIDIEN·Product code GEI·October 26, 2017

    KANGAROO

    FDA Adverse Event
    Malfunction ·MEDTRONIC (FORMERLY COVIDIEN)·Product code KNT·May 10, 2016

    MEDTRONIC PERIPHERAL (FORMERLY COVIDIEN VASCULAR / EV3)

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NIO·September 13, 2022

    TI-CRON 2-0 STR W/10" SWGD NDL BX OF12

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GAT·April 10, 2025

    MEDTRONIC PERIPHERAL (FORMERLY COVIDIEN VASCULAR EV3) GUIDEWIRE

    FDA Adverse Event
    Injury ·MEDTRONIC/COVIDIEN LP·Product code DQX·August 28, 2025

    Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 384400 (US) Intended to provide enteral nutrition to a patient for hospital and acute care settings.

    FDA Recall
    Terminated ·Medtronic·Product code LZH·April 1, 2016

    Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 584400 (OUS) Intended to provide enteral nutrition to a patient for hospital and acute care settings.

    FDA Recall
    Terminated ·Medtronic·Product code LZH·April 1, 2016

    Puritan Bennett 980 Series Ventilator

    FDA Enforcement
    Class I ·Ongoing·Medtronic formerly Covidien·May 4, 2022

    Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT612030V01, CVT808015, CVT808025, CVT812015, CVT812025, EVT808015, EVT808025, EVT812015, EVT812025, BVT808015, BVT808030, BVT812015, BVT812030, EUT808015, EUT808030, EUT812015, EUT812030. Product Usage: The Trellis 6 and Trellis 8 peripheral infusion system is intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.

    FDA Recall
    Terminated ·Medtronic Inc. Cardiac Rhythm Disease Management·Product code KRA·March 23, 2015

    UNKNOWN MICRO CATHETERS

    FDA Adverse Event
    Injury ·IRVINE·Product code KRA·June 12, 2015

    Puritan Bennett 980 Series Ventilator

    FDA Recall
    Open, Classified ·Medtronic formerly Covidien Michael Collins Road, Mervue Ind. Park Galway Ireland·Product code CBK·March 25, 2022

    ONYX AVM

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code MFE·June 12, 2015

    PURITAN BENNETT BB980 VENTILATOR SYSTEM

    FDA Adverse Event
    Malfunction ·COVIDIEN / MEDTRONIC, FORMERLY NELLCOR PURITAN BENNETT, INC.·Product code CBK·November 28, 2018

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Malfunction ·MEDTRONIC/COVIDIEN FORMERLY MICRO THERAPEUTICS, INC. DBA EV·Product code OUT·November 14, 2016

    Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT612030V01, CVT808015, CVT808025, CVT812015, CVT812025, EVT808015, EVT808025, EVT812015, EVT812025, BVT808015, BVT808030, BVT812015, BVT812030, EUT808015, EUT808030, EUT812015, EUT812030. Product Usage: The Trellis 6 and Trellis 8 peripheral infusion system is intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.

    FDA Enforcement
    Class II ·Terminated·Medtronic Inc. Cardiac Rhythm Disease Management·April 8, 2015