Device recall
Z-2395-2012: Empty Evacuated Container 250 mL and 1000 mL. Empty Evacuated containers are…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-2395-2012 |
|---|---|
| Recall event | 63078 |
| Product | Empty Evacuated Container 250 mL and 1000 mL. Empty Evacuated containers are used for mixing compatible medications or blood collections. |
| Product code | KPE |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2013 |
| FEI number | 3013319212 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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