Device recall
Z-2671-2011: B. Braun Celsite Venous Access Ports, Distributed by Aesculpa Inc. Model ST301…
FDA device recall · Class II · B. Braun Interventional Systems
Key facts
| Recall number (Z-number) | Z-2671-2011 |
|---|---|
| Recall event | 58718 |
| Product | B. Braun Celsite Venous Access Ports , Distributed by Aesculpa Inc. Model ST301, ST305V, ST301G, ST501G and ST315 Reference # Model # 04430425 ST301 04430095 ST305V 04433823 ST301G 04437025 ST501G 04436725 ST315 |
| Product code | LJT |
| Recalling firm | B. Braun Interventional Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 6, 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