BEUDAMED
    77 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    BD PYXIS¿ MEDBANK

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 14, 2025

    BD PYXIS¿ MEDBANK

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·February 6, 2026

    BD PYXIS¿ MEDBANK TOWER AUX

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 11, 2025

    BD PYXIS¿ MEDBANK TOWER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 21, 2025

    BD PYXIS¿ MEDBANK TOWER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 11, 2025

    AFFINITY QS Q-SWITCHED ND:YAG LASER SYSTEM

    FDA Adverse Event
    Malfunction ·Product code GEX·July 3, 2014

    BD PYXIS¿ MEDBANK MINI

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 13, 2025

    SURESTEP¿ FOLEY TRAY SYSTEM BARDEX® I.C. COMPLETE CARE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·May 14, 2021

    BD PYXIS¿ MEDBANK TOWER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 5, 2025

    1.8MM Q-FIX ALL SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code MBI·January 15, 2026

    S/5 ANESTHESIA MONITOR

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE FINLAND QY·Product code MHX·March 3, 2009

    COBAS 6000 C (501) MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·December 18, 2025

    FLEXOR ANSEL GUIDING SHEATH

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·September 23, 2021

    UNK HIP FEMORAL STEM TRI-LOCK

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LPH·March 27, 2024

    2517506-2017-00059

    FDA Adverse Event
    Malfunction ·January 19, 2017

    BARDEXLUBRICATH FOLEY CATHETER ALCOCK MODEL

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·June 21, 2021

    RELIAVAC CLOSED WOUND SUCTION EVACUATOR, 100CC

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GCY·November 12, 2020

    BARDEX LUBRICATH FOLEY CATHETER TIEMANN MODEL COUDE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·October 15, 2020

    RELIAVAC CLOSED WOUND SUCTION EVACUATOR, 100CC

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GCY·December 30, 2021

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·April 28, 2023