BEUDAMED
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    Filters Status: Malfunction ×

    SHORT 5MM CANNULA/DILATOR W/RAD ECPD SLV

    FDA Adverse Event
    Malfunction ·PONCE - USS·Product code GCJ·July 1, 2004

    VITEK® 2 AST -P654 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·November 30, 2018

    VITEK® 2 AST -P654 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·November 30, 2018

    VELYS ARRAY SET KNEE

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 3015516266·Product code OLO·August 13, 2024

    VELYS SAW INTERFACE RIGHT

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code HWM·January 18, 2022

    VITEK® 2 AST -P654 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·November 30, 2018

    VITEK® 2 AST -P654 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·November 30, 2018

    1 ML BD SLIP TIP SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 19, 2019

    VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P648 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·March 14, 2018

    VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P632 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·March 21, 2018

    VITEK® 2 AST-P612 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·June 12, 2017

    8X30MM MILAGRO ADVANCE INTERFERENCE SCREW

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code HWC·January 26, 2018

    VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P654 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·March 21, 2018

    VITEK® 2 AST-P612 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·June 12, 2017

    VITEK 2 AST-P619 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 4, 2019

    AESTIVA 7900

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·April 3, 2019

    ATLAS PLUS DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·January 22, 2014

    EPIC DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·November 4, 2013

    ETHICON BIPOLAR CABLE

    FDA Adverse Event
    Malfunction ·ETHICON·Product code IKD·May 21, 2001

    EPIC PLUS VR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·February 27, 2014