BEUDAMED
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    MIC-KEY LOW - PROFILE JEJUNAL FEEDING TUBE

    FDA Adverse Event
    Injury ·HALYARD HEALTH·Product code KNT·December 12, 2017

    MIC-KEY LOW - PROFILE JEJUNAL FEEDING TUBE

    FDA Adverse Event
    Malfunction ·HALYARD HEALTH·Product code KNT·December 12, 2017

    MIC-KEY* LOW - PROFILE JEJUNAL FEEDING TUBE

    FDA Adverse Event
    Injury ·HALYARD HEALTH·Product code KNT·December 11, 2017

    MIC-KEY* JEJUNAL FEEDING TUBE

    FDA Adverse Event
    Death ·HALYARD HEALTH·Product code KNT·December 11, 2017

    COAGULATION FACTOR VIII DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·September 17, 2024

    COAGULATION FACTOR VIII DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·September 13, 2024

    COAGULATION FACTOR VIII DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·October 24, 2025

    COAGULATION FACTOR VIII DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·March 3, 2017

    COAGULATION FACTOR IX DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCT GMBH·Product code GJT·September 19, 2018

    COAGULATION FACTOR IX DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCT GMBH·Product code GJT·September 19, 2018

    COAGULATION FACTOR IX DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCT GMBH·Product code GJT·September 19, 2018

    COAGULATION FACTOR IX DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCT GMBH·Product code GJT·September 19, 2018

    COAGULATION FACTOR IX DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCT GMBH·Product code GJT·September 19, 2018

    CLOTTING FACTOR V DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·March 13, 2020

    COAGULATION FACTOR IX DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·December 6, 2013

    COAGULATION FACTOR IX DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·December 6, 2013

    COAGULATION FACTOR IX DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·December 6, 2013

    COAGULATION FACTOR VIII DEFICIENT PLASMA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJT·January 4, 2018

    Factor deficient plasma for the Siemens BCS / BCS XP System. In vitro diagnostic reagent for the determination of the activity of coagulation factor IX in human plasma by coagulometric methods.

    FDA Recall
    Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code GJT·May 11, 2015

    Vial Label: 1) LIATEST VWF:Ag Buffer - 5 ml Diagnostica Stago 2) LIATEST VWF:Ag Latex + 4 ml R3 Diagnostica Stago 3) LIATEST VWF:Ag Latex Diluent 4 mL Diagnostica Stago Model, catalogue, number 00518 - 58978 - 58979 Kit Label: LIATEST VWF:Ag DIAGNOSTICA STAGO S.A.S. 92600 Asnires sur Seine (France) Coagulation Assay

    FDA Recall
    Terminated ·Diagnostica Stago, Inc.·Product code GJT·January 28, 2013