BEUDAMED
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    ASSAYED EXTERNAL CONTROL MATERIAL FOR MICROBIOLOGY NUCLEIC ACID AMPLIFICATION

    FDA Adverse Event
    Malfunction ·MICROBIOLOGICS INC.·Product code PMN·March 9, 2023

    VITEK® 2 AST-GP67 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 5, 2019

    ID NOW COVID-19 2.0 TEST KIT 24T OUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 24, 2023

    COULTER® 4C® PLUS CELL CONTROL

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JPK·May 18, 2011

    EVIS EXERA III COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·June 5, 2024

    BD VACUTAINER® MICROBIOLOGY C&S TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 18, 2018

    SYSTEM 2000

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code ILJ·April 28, 2017

    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·December 11, 2018

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 5, 2021

    4C -ES CELL CONTROL

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JPK·June 15, 2011

    ID NOW COVID-19 2.0 TEST KIT 24T OUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 26, 2023

    ID NOW COVID-19 2.0 TEST KIT 24T OUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 26, 2023

    ID NOW COVID-19 2.0 TEST KIT 24T OUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 26, 2023

    ID NOW COVID-19 2.0 TEST KIT 24T OUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 26, 2023

    BARDEX® LUBRI-SIL® I.C. TEMPERATURE-SENSING ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·January 4, 2019

    DXH HEMATOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·December 1, 2011

    HISTOACRYL BLUE 0.5ML

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL SA·Product code MPN·November 21, 2018

    ALLERGAN CUP (GORTEX)

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LPN·September 23, 2020

    ALLERGAN CUP (GORTEX)

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LPN·October 16, 2020

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 15, 2021