Device recall
Z-0162-2011: IV Catheter - Optiva IV Catheter. This is found in box labeled 'Graft Jacket…
FDA device recall · Class II · LifeCell Corporation
Key facts
| Recall number (Z-number) | Z-0162-2011 |
|---|---|
| Recall event | 56826 |
| Product | IV Catheter - Optiva IV Catheter. This is found in box labeled 'Graft Jacket Xpress Flowable Soft Tissue Scaffold'; labeled by Wright. |
| Product code | KGZ |
| Recalling firm | LifeCell Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 17, 2012 |
| FEI number | 1000306051 |
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