78 results
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51ms
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Sources: EU EUDAMED, US FDA
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
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
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
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
Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.
FDA Recall
Open, Classified
·C.A. Greiner & Sohne Gesellschaftmbh Greiner St. # 70 Kremsmunster Austria·Product code FMI·July 27, 2020
VACUETTE TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged
FDA Recall
Open, Classified
·Greiner Bio-One North America, Inc.·Product code JKA·May 14, 2024
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 tube 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged - Product Usage: indicated for use in collection and transport of venous whole blood for coagulation testing.
FDA Recall
Terminated
·Greiner Bio-One North America, Inc.·Product code GIM·March 29, 2021
GREINER VACUETTE
FDA Adverse Event
Malfunction
·GREINER VACUETTE NORTH AMERICA, INC·Product code JKA·August 8, 2000
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