BEUDAMED
    12 results · 28ms · Sources: EU EUDAMED, US FDA

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    MICROTAINER SST GOLD

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·June 7, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 1, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 16, 2018

    MICROTAINER SST GOLD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD·Product code JKA·May 7, 2018

    BD MICROTAINER® EDTA LAVENDER TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·April 27, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 3, 2018

    BD MICROTAINER® BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·December 3, 2017

    COBAS 8000 E602 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 11, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·November 29, 2010

    INGENIO

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 3, 2014

    VITEK® 2 GRAM NEGATIVE IDENTIFICATION TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LQM·September 13, 2018

    VITEK® 2 GRAM NEGATIVE IDENTIFICATION TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LQM·September 13, 2018