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

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    Filters FDA Recall × Status: Terminated × Clear all

    Acacia Catalog # 385166 Dual "Y" IV Extension Set 50cm Macro Bore, Spin Nut w/BD Q-Syte

    FDA Recall
    Terminated ·Medical Product Specialist Inc dba MPS Acacia·Product code FPA·December 18, 2009

    Acacia Catalog # 385150 IV Extension Set 15cm Small Bore, Spin Nut w/BD Q-Syte

    FDA Recall
    Terminated ·Medical Product Specialist Inc dba MPS Acacia·Product code FPA·December 18, 2009

    Acacia Catalog # 385151 IV Extension Set 15cm Small Bore, Spin Nut w/BD Q-Syte

    FDA Recall
    Terminated ·Medical Product Specialist Inc dba MPS Acacia·Product code FPA·December 18, 2009

    Acacia Catalog # 385164 Tri-Extension IV Set 15cm Small Bore, Spin Nut w/BD Q-Syte

    FDA Recall
    Terminated ·Medical Product Specialist Inc dba MPS Acacia·Product code FPA·December 18, 2009

    Acacia Catalog # 385165 "Y" IV Extension Set 20cm Macro Bore, Spin Nut w/BD Q-Syte

    FDA Recall
    Terminated ·Medical Product Specialist Inc dba MPS Acacia·Product code FPA·December 18, 2009

    MPS Acacia Extension Set, 15cm Small Bore, Spin Nut w/BD Q-Syte, REF 385151

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

    MPS Acacia Tri-Extension Set, 15cm Small Bore, Spin Nut w/BD Q-Syte, REF 385164

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

    BD Q-Syte Vial Access Adapter, 0.16 ml, REF 385108, Becton Dickinson Infusion Therapy Systems Inc.

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

    BD Q-Syte, Luer Access Split-Septum, 0.10 ml, REF 385100, Becton Dickinson Infusion Therapy Systems Inc.

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

    BD Q-Syte Extension Set, 15 cm, P.V. 0.21 ml, REF 385102, Becton Dickinson Infusion Therapy Systems Inc.

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

    Medical Action Industries, Dialysis Kit, using BD Q-Syte Luer Access Split Septum (BD #385100), Part number: 57977.

    FDA Recall
    Terminated ·Medical Action Industries Inc·Product code FPA·November 6, 2009

    Medical Action Industries, Venous Access Tray, using BD Q-Syte Luer Access Split Septum (BD #385100)), Part number: 69498.

    FDA Recall
    Terminated ·Medical Action Industries Inc·Product code FPA·November 6, 2009

    Medical Action Industries, IV Start Bundle Kit, using MPS Acacia with BD Q-Syte (BD #385151), Part number: 69946B.

    FDA Recall
    Terminated ·Medical Action Industries Inc·Product code FPA·November 6, 2009

    BD Q-Syte Extension Set, 15cm Std Bore, P.V. 1.14 ml Luer-Lok, REF 385101, Becton Dickinson Infusion Therapy Systems Inc.

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

    BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc. An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code FPA·February 19, 2015

    Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The BUN method is an in vitro diagnostic test for the quantitative measurement of urea nitrogen (an end product of nitrogen metabolism) in human serum, plasma, and urine on the Dimension Vista System.

    FDA Recall
    Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code CDQ·February 16, 2016

    ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use on ADVIA 1800, 2400 and XPT Chemistry Systems

    FDA Recall
    Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code CDQ·March 27, 2018

    Tina-quant IgM Gen.2, Catalog Nos. 03507190190, 05220726190, 03507041190, 03507149190 Product Usage: Immunoturbidimetric assay for the quantitative in vitro determination of IgM in human serum and plasma on automated clinical chemistry analyzers analyzers.

    FDA Recall
    Terminated ·Roche Diagnostics Corporation·Product code DAQ·December 17, 2018

    Clinical Chemistry Urea Nitrogen List Number 7D75-21 and 7D75-31 used for the Quantitation of urea nitrogen in human serum, plasma, and urine.

    FDA Recall
    Terminated ·Abbott Laboratories, Inc·Product code CDQ·October 3, 2011

    AEROSET/ARCHITECT c8000 Urea Nitrogen Models: 7D75-01; 7D75-20; 7D75-30

    FDA Recall
    Terminated ·Abbott Laboratories Diagnostic Div·Product code CDQ·November 24, 2003