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    GREINER BIO-ONE NORTH AMERICA, INC.

    FDA registration
    GREINER BIO-ONE NORTH AMERICA, INC.·5 products·🇺🇸 United States

    3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc., 4238 Capital Drive, Monroe, NC 28110. Intended Use: Venous blood collection tubes.

    FDA Enforcement
    Class II ·Terminated·Greiner Bio-One North America, Inc.·August 15, 2012

    Vacuette 2 ml Lithium Heparin, Collection Tube, Manufactured by: Greiner-Bio One North America, Inc., 4238 Capital Drive, Monroe, NC. Venous blood collection tubes.

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code JKA·August 25, 2010

    3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc., 4238 Capital Drive, Monroe, NC 28110. Intended Use: Venous blood collection tubes.

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code GIM·July 2, 2012

    VACUETTE, 2 ml Lithium Heparin Venous Blood Collection Tubes. Reference #454237, 13x75 green cap-white ring, 24 racks of 50 pcs (1200 pcs in total, non ridged, Sterile). Manufactured by: Greiner bio-one NA, Inc., 4238 Capital Drive, Monroe, NC 28110. The Greiner Vacuette blood collection tube with lithium heparin and gel separator is an evacuated blood collection device containing lithium heparin, an anticoagulant additive, and an inert polymeric barrier material. The product is intended for use in holding and separating blood plasma from the cellular components of blood.

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code JKA·July 29, 2008

    Greiner bio-one * Vacuette Tube * 9C Coagulation Sodium, Citrate 3.2%, * 3.5mL * blue cap-black ring * 24 racks of 50, 1200 pcs in total * non-ridged * Sandwich Tube * 454332 * B050609 * 2007-05 * Sterile * manufactured by: Greiner Bio-one North America, Inc., 4238 Capital Drive, Monroe, NC 28110, USA

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code GIM·August 2, 2006

    HOLDEX Single-Use Holder PP closed pack. Greiner Bio-One Austria Gmbh. A sterile single-use disposable holder with an off-center female luer at the top of the holder and epoxy bonded stainless steel needle on the underside of the holder, recommended for use with commercially available butterfly and luer needles in routine venipuncture procedures.

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code FMI·June 29, 2011

    Plastic Cannula Holdex Tube Holder, Item number: 450216. It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code FMI·August 5, 2008

    4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an antiglycolytic agent, sodium fluoride, and an anticoagulant, potassium oxalate. The product is suitable for the analysis of blood glucose and lactate

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code JKA·April 26, 2016

    Greiner Bio-One VACUETTE TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code GIM·August 20, 2021

    VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code GIM·March 12, 2020

    VACUETTE BLOOD COLLECTION TUBES WITH SODIUM CITRATE

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA, INC.·Product code GIM·June 21, 2012

    VACUETTE QUICKSHIELD SAFETY TUBE HOLDER

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA, INC.·Product code FMI·May 18, 2022

    GREINER BIO-ONE VACUETTE QUICKSHIELD COMPLETE PLUS

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA INC.·Product code FMI·August 20, 2015

    SAFETY BLOOD COLLECTION SET AND HOLDER

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA, INC.·Product code FMI·July 3, 2024

    VACUETTE

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA, INC.·Product code JKA·January 31, 2014

    VACUETTE QUICKSHIELD

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA, INC·Product code JKA·July 23, 2014

    VACUETTE SAFETY BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA, INC.·Product code FMI·August 11, 2014

    VACUETTE

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA, INC.·Product code FMI·November 20, 2018

    GRINER NEEDLE

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NORTH AMERICA, INC.·Product code FMI·September 5, 2023