Device recall
Z-1961-2009: Celsite Access Port Model ST305P. The Celsite Access Port model ST305P is a…
FDA device recall · Class II · B. Braun Interventional Systems
Key facts
| Recall number (Z-number) | Z-1961-2009 |
|---|---|
| Recall event | 52611 |
| Product | Celsite Access Port Model ST305P. The Celsite Access Port model ST305P is a member of the Celsite product line of implantable port and catheter systems. |
| Product code | LJT |
| Recalling firm | B. Braun Interventional Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 5, 2012 |
| 510(k) numbers | K061424 |
| FEI number | 3006332832 |
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