BEUDAMED
    43 results · 52ms · Sources: EU EUDAMED, US FDA

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    ET-20 Anesthesia Extension Tubes, 2.5 ml approximately, Sterile and Disposable, Wall Medical Inc., Made in China

    FDA Recall
    Terminated ·Global Healthcare Inc·Product code FPA·January 6, 2016

    MED 5223 - VacuFlow Safe, Multi-Sample Blood Collection Set With Luer Adapter Tube 12", Sterile, Rx only, Distributed by Tanner Scientific, Sarasota, FGL 34243 Made in China.

    FDA Recall
    Terminated ·Global Healthcare Inc·Product code FMI·August 9, 2016

    MED 5223 - VacuFlow Safe, Multi-Sample Blood Collection Set With Luer Adapter Tube 12", Sterile, Rx only, Distributed by Tanner Scientific, Sarasota, FGL 34243  Made in China.

    FDA Enforcement
    Class II ·Terminated·Global Healthcare Inc·September 28, 2016

    ET-20 Anesthesia Extension Tubes, 2.5 ml approximately, Sterile and Disposable, Wall Medical Inc., Made in China

    FDA Enforcement
    Class II ·Terminated·Global Healthcare Inc·February 10, 2016

    UNK

    FDA Adverse Event
    Death ·*·Product code JEA·September 22, 2006

    ADVIA 1800

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·October 3, 2013

    ADVIA CENTUAR XP SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·February 19, 2018

    SYNVISC ONE

    FDA Adverse Event
    Malfunction ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·November 17, 2017

    AQUACEL AG-EXUDATE MANAGEMENT HYDROFIBER

    FDA Adverse Event
    Injury ·CONVATEC LIMITED·Product code NAC·February 28, 2014

    ALPHAXCELL

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH, A BRANCH OF ARJO LTD MED AB·Product code IKY·July 17, 2012

    DURAGEN-UNKNOWN PRODUCT ID

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·August 24, 2018

    BCS XP SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GKP·September 29, 2017

    Hospira Phoenix Infusion System with MedNet Software, Symbiq One-Channel Infusion System, Software versions v2.1 & v3.0, Manufactured by Hospira Inc., Morgan Hill, CA.

    FDA Recall
    Terminated ·Hospira Inc·Product code frn·March 31, 2009

    Hospira Phoenix Infusion System with MedNet Software, Symbiq Two-Channel Infusion System, Software versions v2.1 & v3.0, Manufactured by Hospira Inc., Morgan Hill, CA

    FDA Recall
    Terminated ·Hospira Inc·Product code frn·March 31, 2009

    XPS® BLADE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·January 30, 2023

    FLOWTRON EXCEL/TRIO PUMPS

    FDA Adverse Event
    Other ·GETINGE (SUZHOU) CO. LTD.·Product code JOW·July 25, 2012

    FLOWTRON/UNIVERSAL PUMPS

    FDA Adverse Event
    Malfunction ·GETINGE (SUZHOU) CO. LTD.·Product code JOW·July 17, 2012

    Spacelabs Pediatric Flow Sensor Kit, PN: 376-0561-00. This kit is for Spacelabs Healthcare Blease 700/900 Series Ventilators. Designed specifically for the mechanical ventilation of adult and pediatric patients under general anesthesia.

    FDA Recall
    Terminated ·Del Mar Reynolds Medical, Ltd.·Product code CBK·March 5, 2015

    Flow Coupler Monitor, GEM, Global Excellence Microsurgery, Rx Only

    FDA Recall
    Open, Classified ·Baxter Healthcare Corporation·Product code MVR·June 2, 2020

    GAMIDA

    Importer
    🇫🇷 France·5 Manufacturers