Greiner Bio-One North America, Inc.
3 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Greiner Bio-One North America, Inc. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2024-07-24FDA-DeviceClass IIVACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged
The firm received reports that some blood collection tubes have experienced issues with clotting and poor separation due to missing additive. The failure of the device would likely require sample recollection which could result in a delay of treatment.
- 2024-01-24FDA-DeviceClass IIVACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate, Item #454297, 13x75 grey cap-black ring, non-ridged.
Tubes have missing additive/anticoagulant resulting in clotting in most cases. A completely clotted sample would lead to no results being reported, which could lead to a delay in treatment or diagnosis. An erroneous glucose or lactose result from a partially clotted sample could lead to inappropriate treatment.
- 2023-05-24FDA-DeviceClass IIgreiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA, 13x100 pink cap-black ring, non-ridged, 24 racks of 50 pcs., 1200 pcs in total, Item #456003
Some of the tubes may be incorrectly labeled.
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