Device recall
Z-0264-2008: Vena Tech LP Vena Cava Filter System, Item No/REF. 05010024, Model No: 40DLP, B…
FDA device recall · Class II · B. Braun Interventional Systems
Key facts
| Recall number (Z-number) | Z-0264-2008 |
|---|---|
| Recall event | 45539 |
| Product | Vena Tech LP Vena Cava Filter System, Item No/REF. 05010024, Model No: 40DLP, B Braun. Manufacturer: B. Braun Medical 204, avenue du Marechal Juin BP 331 92107 Boulogne Cedex , France. (The VenaTech LP vena cava filter is pre-loaded in a syringe (cartridge) and provided as a system with introducer… |
| Product code | DTK |
| Recalling firm | B. Braun Interventional Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 2, 2008 |
| 510(k) numbers | K010485, K063217 |
| FEI number | 3006332832 |
At a glance
- 1–9 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