BEUDAMED
    7,997 results · 103ms · Sources: EU EUDAMED, US FDA

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    MINISCAV (tm) Vacuum Pump

    FDA Enforcement
    Class II ·Ongoing·R A Medical Services·September 27, 2023

    MINISCAV (tm) Vacuum Pump

    FDA Recall
    Open, Classified ·R A Medical Services Holmes House Skipton Road Keighley United Kingdom·Product code BTA·August 23, 2023

    TELIGEN

    FDA Adverse Event
    Death ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·June 29, 2012

    CORDIS

    FDA Adverse Event
    Injury ·CORDIS, INC.·Product code DYB·October 24, 1994

    RESONATE X4 CRT-D

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIK·March 7, 2023

    COBAS AMPLIPREP / COBAS TAQMAN HIV-1 TEST

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS·Product code MZF·September 28, 2010

    ONE TOUCH LANCING DEVICE

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·October 15, 2010

    DIMENSION® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Injury ·SIEMENS HEALTHCARE DIAGNOSTICS INC- BROOKFIELD·Product code JJE·April 19, 2011

    TITANIUM GREENFIELD FILTER

    FDA Adverse Event
    Malfunction ·MEDITECH·Product code DTK·June 2, 1992

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·August 1, 2025

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 15, 2024

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 15, 2024

    CHARIOT AMBULATOR

    FDA Adverse Event
    Injury ·FIRST CHOICE INTERNATIONAL·Product code FKX·September 22, 1992

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·February 20, 2012

    TVL-ADX ACTIVE-FIXATION STEROID-ELUTING TACHYARRHYTHMIA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·April 27, 2006

    PCA IMPLANT

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code HRY·July 8, 1992

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 15, 2024

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 15, 2024

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code MEA·February 15, 2024

    GALILEO

    FDA Adverse Event
    Other ·IMMUCOR, INC.·Product code KSZ·August 30, 2006