Device recall
Z-2699-2011: LIFECATH S PICC Catheter, Percutaneous, Intravascular Product Code 2296.211…
FDA device recall · Class II · Vygon Corporation
Key facts
| Recall number (Z-number) | Z-2699-2011 |
|---|---|
| Recall event | 58810 |
| Product | LIFECATH S PICC Catheter, Percutaneous, Intravascular Product Code 2296.211 Product Usage:: Intravascular catheter |
| Product code | LJS |
| Recalling firm | Vygon Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 1, 2012 |
| 510(k) numbers | K062425 |
| FEI number | 2245270 |
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