BEUDAMED
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    Filters FDA Adverse Event × Status: Malfunction × Clear all

    SLIDEPREP PLUS CYTOLOGY CENTRIFUGE

    FDA Adverse Event
    Malfunction ·SEPARATION TECHNOLOGY, INC.·Product code JQC·December 19, 2012

    SLIDEPREP PLUS CYTOLOGY CENTRIFUGE

    FDA Adverse Event
    Malfunction ·SEPARATION TECHNOLOGY, INC. PART OF THERMO FISHER SCIENTIFIC·Product code IFB·August 16, 2012

    CLEAR-CRIT PLASTIC CAPILLARY TUBES

    FDA Adverse Event
    Malfunction ·SEPARATION TECHNOLOGY, INC.·Product code GIO·October 28, 1999

    STAT-60

    FDA Adverse Event
    Malfunction ·SEPARATION TECHNOLOGY, INC.·Product code JQC·November 8, 2002

    VANISHPOINT

    FDA Adverse Event
    Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·December 11, 2015

    8.5F SHEATH WITH CURVE VIZ MDC

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code LPB·April 8, 2019

    SLIDEPREP PLUS CYTOLOGY CENTRIFUGE

    FDA Adverse Event
    Malfunction ·SEPARATION TECHNOLOGY, INC., PART OF THERMO FISHER SCIENTIFIC·Product code JQC·May 1, 2013

    SLIDEPREP PLUS CYTOLOGY CENTRIFUGE

    FDA Adverse Event
    Malfunction ·SEPARATION TECHNOLOGY, INC., PART OF THERMO FISHER SCIENTIFIC·Product code JQC·August 30, 2012

    PREMILENE NON-CARDIOVASCULAR

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAW·February 19, 2018

    AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC

    FDA Adverse Event
    Malfunction ·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022

    AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC

    FDA Adverse Event
    Malfunction ·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022

    CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ MEDIUM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·April 4, 2019

    CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH -

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·April 16, 2019

    INTELISWAB COVID-19 RAPID TEST

    FDA Adverse Event
    Malfunction ·ORASURE TECHNOLOGIES INC.·Product code QKP·January 6, 2022

    AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC

    FDA Adverse Event
    Malfunction ·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022

    WEBSTER CS CATHETER WITH AUTO ID TECHNOLOGY

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·May 9, 2025

    INTELISWAB COVID-19 RAPID TEST

    FDA Adverse Event
    Malfunction ·ORASURE TECHNOLOGIES, INC.·Product code QKP·November 29, 2023

    INTELISWAB COVID-19 RAPID TEST

    FDA Adverse Event
    Malfunction ·ORASURE TECHNOLOGIES, INC.·Product code QKP·November 29, 2023

    INTELISWAB COVID-19 RAPID TEST

    FDA Adverse Event
    Malfunction ·ORASURE TECHNOLOGIES, INC.·Product code QKP·November 29, 2023

    ON-X ASCENDING AORTIC PROSTHESIS

    FDA Adverse Event
    Malfunction ·CRYOLIFE, INC. ¿ AUSTIN·Product code LWQ·October 4, 2016