BEUDAMED
    5 results · 51ms · Sources: EU EUDAMED, US FDA

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    MEDIPORT CATHETER

    FDA Adverse Event
    BARD ACCESS SYSTEMS, INC.·Product code LJT·August 8, 1995

    MONOLERT

    FDA Adverse Event
    Malfunction ·MERIDIAN DIAGNOSTICS, INC.·Product code LJN·January 4, 1995

    PARA-PAK/PARA-PAK ULTRA ECO FIX SYSTEM

    FDA Adverse Event
    Death ·MERIDIAN DIAGNOSTICS, INC.·Product code JSM·November 29, 2000

    Bio-Rad brand Meridian ANA Screen ELISA Test Kit, 96 Test, Catalog No. 4884261, Manufactured by: Bio-Rad Laboratories, Inc. Hercules, CA and distributed by Meridian Diagnostics.

    FDA Recall
    Terminated ·Bio-Rad Laboratories Inc·Product code LKJ·February 24, 2010

    Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300

    FDA Recall
    Open, Classified ·Meridian Bioscience Inc·Product code OZN·December 5, 2025