Greiner Bio-One North America, Inc.: 7 recalls on record

Recalls filed with 1 agency: FDA (7).

First recall on record: July 11, 2012. Most recent: July 24, 2024.

Risk classification: Class II: 7

Most recent recalls

DateAgencyProduct
July 24, 2024FDAVACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-r…Z-2375-2024
January 24, 2024FDAVACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate, Item #454297, 13x75 grey cap-bla…Z-0733-2024
January 26, 2022FDAgreiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring,…Z-0502-2022
April 22, 2020FDAVACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.Z-1714-2020
February 27, 2013FDAVACUETTE Safety Blood Collection Set + Luer Adapter, 23x12" Safety Blood Collect LA Produ…Z-0835-2013
August 15, 2012FDA3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc…Z-2154-2012
July 11, 2012FDAVacuette Quickshield Complete Plus, 21G x 1 (0.8 x 25 mm), Greiner bio-one. The Quick…Z-1935-2012

Questions about this company

How many recalls does Greiner Bio-One North America, Inc. have?
Recalert has 7 U.S. recalls on record for Greiner Bio-One North America, Inc., published between July 11, 2012 and July 24, 2024.
What was the most recent Greiner Bio-One North America, Inc. recall?
FDA recall Z-2375-2024, published July 24, 2024: VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged
Which agencies have handled Greiner Bio-One North America, Inc. recalls?
Greiner Bio-One North America, Inc. appears as the recalling firm in recalls from: FDA (7).

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