BEUDAMED
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    Filters Status: Malfunction ×

    ENDO KIT

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRUIES LP·Product code NWR·November 2, 2021

    SILICONE FOLEY CATHETER, 14F

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, INC.·Product code NWR·July 11, 2014

    ENDO KIT

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRUIES LP·Product code NWR·November 2, 2021

    LUBRICATH

    FDA Adverse Event
    Malfunction ·CR BARD·Product code NWR·September 8, 2016

    KIT, CATHETER, FOLEY

    FDA Adverse Event
    Malfunction ·C.R. BARD·Product code NWR·July 7, 2017

    *

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES·Product code NWR·November 25, 2013

    ERASE CAUTI

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, INC.·Product code NWR·November 26, 2013

    ERASE CAUDI

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, INC·Product code NWR·November 15, 2013

    SILICONE TOTAL ONE LAYER FOLEY CATHETER TRAY

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES INC·Product code NWR·May 25, 2016

    SURESTEP FOLEY TRAY SYSTEM

    FDA Adverse Event
    Malfunction ·BARD MEDICAL·Product code NWR·April 7, 2015

    HSCT KOR IV SET TPE GFR SS 5UM P 3W R AP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·February 16, 2021

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·September 3, 2025

    HEAD RING DRIVE (BWR & CRW)

    FDA Adverse Event
    Malfunction ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·January 27, 2012

    LEVEMIR FLEXPEN 100U/ML

    FDA Adverse Event
    Malfunction ·NOVO NOR INC·Product code FMF·May 22, 2008

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·February 2, 2024

    NOR-AM

    FDA Adverse Event
    Malfunction ·NOR-AM PATIENT CARE PRODUCTS·Product code FNG·June 6, 2008

    PERCEPT

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·February 13, 2026

    READY LIFT

    FDA Adverse Event
    Malfunction ·NOR-AM PATIENT CARE PRODUCTS LTD.·Product code FNG·August 27, 1998

    ROTABLATOR GUIDE WIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP./NW TECHNOLOGY CENTER·Product code DQX·June 13, 2000

    MMSI FINAL TIGHTENER

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES SPINE·Product code HWR·October 7, 2016