Recall Z-0086-06 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Greiner VACUETTE North America
Serum Blood Collection Tubes
| Date | Oct 22, 2005 (initiated Jul 28, 2005) |
| Status | Terminated |
| Reason | Serum Blood Collection tubes found with excess of Blood Clot Accelerator (BCA) solution. |
| Root cause | Other |
| Action | Consignees were notified by letter on 07/28/2005. |
| Quantity | 1623 cases (1,947,600 pieces) |
| Distribution | Nationwide, Chile, Costa Rica, Ecuador, El Salvador, Nicaragua and Uruguay. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K960858 | GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR Greiner America, Inc., Aug 30, 1996 |