Device recall
Z-0215-2009: VACUETTE, 2 ml Lithium Heparin Venous Blood Collection Tubes. Reference #454237…
FDA device recall · Class III · Greiner Bio-One North America, Inc.
Key facts
| Recall number (Z-number) | Z-0215-2009 |
|---|---|
| Recall event | 49371 |
| Product | 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… |
| Product code | JKA |
| Recalling firm | Greiner Bio-One North America, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 26, 2009 |
| 510(k) numbers | K960857 |
| FEI number | 3001451379 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database