Device recall
Z-2154-2012: 3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North…
FDA device recall · Class II · Greiner Bio-One North America, Inc.
Key facts
| Recall number (Z-number) | Z-2154-2012 |
|---|---|
| Recall event | 62595 |
| Product | 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. |
| Product code | GIM |
| Recalling firm | Greiner Bio-One North America, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2013 |
| 510(k) numbers | K971221 |
| FEI number | 3001451379 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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