Device recall
Z-2191-2008: Vital Port Vascular Access System Polysulfone Petite with detached 1.0mm…
FDA device recall · Class II · Cook Vascular Inc.
Key facts
| Recall number (Z-number) | Z-2191-2008 |
|---|---|
| Recall event | 48642 |
| Product | Vital Port Vascular Access System Polysulfone Petite with detached 1.0mm catheter |
| Product code | LJT |
| Recalling firm | Cook Vascular Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2008 |
| 510(k) numbers | K924748 |
| FEI number | 2522007 |
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