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    Medline Latex Free Labor Kit & Postpartum CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060

    FDA Recall
    Terminated ·Medline Industries Inc·Product code OHM·August 4, 2008

    Medline Latex Free C-Section CDS-LF and C-Section Supplemental CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060

    FDA Recall
    Terminated ·Medline Industries Inc·Product code OHM·August 4, 2008

    Medline Latex Free Vaginal Delivery CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060

    FDA Recall
    Terminated ·Medline Industries Inc·Product code OHM·August 4, 2008

    Medline Latex Free Labor & Delivery CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060

    FDA Recall
    Terminated ·Medline Industries Inc·Product code OHM·August 4, 2008

    Medline Latex Free Mom/Baby Admit Kit - LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060

    FDA Recall
    Terminated ·Medline Industries Inc·Product code OHM·August 4, 2008

    Human Cardiac Specific Fatty Acid-Binding Protein (H-FABP) ELISA TEST KIT Product is an In Vitro Device (IVD) categorized as a Cardiac Marker, manufactured and distributed by BioCheck, Inc., Foster City, CA. Enzyme Immunoassay for the quantitative determination of Human Cardiac Fatty Acid-Binding Protein (H-FABP) concentration in serum, citrate-plasma, EDTA-plasma, and heparin-plasma.

    FDA Recall
    Terminated ·BioCheck Inc·Product code NUK·July 15, 2010

    ETI-AB-AUK PLUS kits,REF P001931, DiaSorin S.p.A., 13040 Saluggia (VC), Italy, Distributed by: DiaSorin Inc., 1951 Northwestern Avenue, P.O. Box 285, Stillwater, MN 55082-0285 In vitro enzyme immunoassay (EIA) intended for use in the qualitative detection of antibodies to hepatitis B surface antigen (anti-HBs) in human serum or plasma.

    FDA Recall
    Terminated ·Diasorin Inc.·Product code LOM·August 19, 2010

    McKesson Cardiology Hemo

    FDA Recall
    Terminated ·Change Healthcare Israel Ltd. 26, Ha-Rokmim Holon Israel·Product code DQK·March 25, 2019

    Horizon Cardiology Hemo

    FDA Recall
    Terminated ·Change Healthcare Israel Ltd. 26, Ha-Rokmim Holon Israel·Product code DQK·March 25, 2019

    12F MODIFIED Tesio CATHETER SET, REF MCTC1235SM, UDI 884908027259 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    12F X 60CM TESIO CATHETER SET WITH "Y" ADAPTOR, REF CMD757, UDI 884908005554 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    INFUSE Bone Graft X SMALL KIT REF 7510100

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·September 27, 2018

    INFUSE(R) Bone Graft, SMALL KIT, REF 7510200, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013

    CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    NextStep Retrograde Replacement Hub Set - Product Usage: is indicated for use in the replacement of a NextStep Retrograde hub connection assembly that has been damaged.

    FDA Recall
    Terminated ·Arrow International Inc·Product code NFK·July 6, 2020

    12F Tesio CATHETER SET (CUFF 22CM FROM TIP), REF MCTC1235SD, UDI 884908027242 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    REPAIR KIT, REF ARA101, UDI 884908083637 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    REPAIR KIT, REF RPK-01, UDI 884908039856 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    CATHETER REPAIR KIT, REF RMS52001, UDI 884908039658 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    INFUSE(R) Bone Graft, LARGE KIT, REF 7510600, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013