BEUDAMED
    61 results · 86ms · Sources: EU EUDAMED, US FDA

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    PRIMARY PLUM Y-TYPE BLOOD SET, 200 MICRON FILTER, CLAVE SECONDARY PORT, SECURE L

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·June 13, 2023

    INFUSOMAT SPACE

    FDA Adverse Event
    Injury ·B.BRAUN MELSUNGEN AG·Product code FRN·February 22, 2016

    INFUSOMAT SPACE

    FDA Adverse Event
    Injury ·B.BRAUN MELSUNGEN AG·Product code FRN·February 22, 2016

    INFUSOMAT SPACE

    FDA Adverse Event
    Injury ·B.BRAUN MELSUNGEN AG·Product code FRN·February 22, 2016

    NEOMED NASOGASTRIC/OROGASTRIC FEEDING TUBES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code FPD·March 17, 2026

    NEOMED NASOGASTRIC/OROGASTRIC FEEDING TUBES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code FPD·March 17, 2026

    NEOMED NASOGASTRIC/OROGASTRIC FEEDING TUBES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code FPD·March 18, 2026

    LEVEL 1 FAST FLOW FLUID WARMER

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC·Product code BSB·April 3, 2025

    HOMEPUMP C-SERIES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code MEB·June 12, 2023

    NEURO PACK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code LRO·December 14, 2023

    D-300 IV ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·May 24, 2006

    PSI Knee System- Prosthesis, knee patellofemorotibial, semi-constrained, cemented, polymer/meal/polymer The Zimmer PSI Knee System is indicated as an orthopedic instrument system to assist in the positioning of knee replacement components.

    FDA Recall
    Terminated ·Zimmer CAS·Product code JWH·November 3, 2014

    INFUSOMAT SPACE

    FDA Adverse Event
    Injury ·B.BRAUN MELSUNGEN AG·Product code FRN·February 22, 2016

    SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·August 11, 2021

    28 CM (11") APPX 2.5 ML, SET AMBRATO PER INFUSIONE 2 CLAVE® CONNECTOR, PERFORATO

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FMG·July 30, 2019

    Salter Labs Bubble humidifier, with 6 PSI safety valve, 350cc, Latex Free; Single Patient use; used with supplemental oxygen therapy. Model Numbers 7600-0-50, E7600-0-50, NP7600-0-50 and special order patient kits that contain 7600 humidifiers. Patient kits have brand names of Salter Labs, AdvaCare; Allcare Medical; Memorial Home Services; Therapy Support Inc; Mendo-Lake Home Respiratory Services; MedAssurance Inc.; Abundant Home Care. Product Usage: Humidifier - single patient use. used with supplemental oxygen therapy.

    FDA Recall
    Terminated ·SALTER LABS·Product code BBT·October 21, 2011

    HEMODIALYSIS BLOODLINES

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL INC.·Product code FJK·November 14, 2024

    HEMODIALYSIS BLOODLINES

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL INC.·Product code FJK·November 14, 2024

    HEMODIALYSIS BLOODLINES

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL INC.·Product code FJK·November 14, 2024

    HEMODIALYSIS BLOODLINES

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL INC.·Product code FJK·November 14, 2024