BEUDAMED
    10,000 results · 721ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    BD ALARIS IV INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BD ALARIS/CAREFUSION 303, INC.·Product code FRN·January 12, 2021

    INSYTE AUTOGUARD 20 GA X 1.16IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY (BD)·Product code FOZ·May 1, 2025

    INSYTE AUTOGUARD 20 GA X 1.16IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY (BD)·Product code FOZ·May 1, 2025

    INSYTE AUTOGUARD 20 GA X 1.16IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY (BD)·Product code FOZ·May 1, 2025

    SPECTRUM IQ IV PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·April 20, 2022

    BAXTER SPECTRUM IQ PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 21, 2022

    ACCURYN SMARTFOLEY UO TEMP TRAY SYSTEM 16FR

    FDA Adverse Event
    Malfunction ·POTRERO MEDICAL, INC.·Product code EZL·October 24, 2022

    CADD-SOLIS VIP AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·FRN·Product code FRN·August 28, 2024

    LIFESHIELD TKO ANTI REFLUX DEVICE

    FDA Adverse Event
    Malfunction ·HOSPIRA INC·Product code FPA·January 31, 2011

    VIAL-MATE

    FDA Adverse Event
    Malfunction ·BAXTER INTERNATIONAL INC.·Product code LHI·July 24, 2023

    INFUSOMAT SPACE PUMP

    FDA Adverse Event
    Malfunction ·BRAUN·Product code FRN·January 19, 2013

    JELCO

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMF·March 7, 2025

    TEVADAPTER

    FDA Adverse Event
    Malfunction ·B BRAUN·Product code LHI·August 29, 2014

    BEAR

    FDA Adverse Event
    Injury ·BEAR MEDICAL SYSTEMS·Product code CBK·February 8, 1999

    PURITAN BENNETT

    FDA Adverse Event
    Injury ·MEDIQ PRN·Product code CBK·March 2, 2004

    FUKUDA DENSHI

    FDA Adverse Event
    Death ·MEDIQ/PRN·Product code DSI·August 31, 2000

    BAXTER

    FDA Adverse Event
    Malfunction ·MEDIQ PRN·Product code FRN·December 12, 2001

    IMED

    FDA Adverse Event
    Malfunction ·MEDIQ - PRN·Product code LZG·May 21, 2001

    SYNERGY AIR II (RENTED)

    FDA Adverse Event
    Injury ·MEDIQ PRN·Product code INX·May 14, 2002

    INFUSION DEVICE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD IN·Product code MEA·September 30, 2013