Device recall
Z-0764-2010: Percutaneous Catheter Introducer Set, VNUS Medical Technologies Cath Shth Intro…
FDA device recall · Class III · Argon Medical Devices, Inc
Key facts
| Recall number (Z-number) | Z-0764-2010 |
|---|---|
| Recall event | 54172 |
| Product | Percutaneous Catheter Introducer Set, VNUS Medical Technologies Cath Shth Intro 7F x 7cm, catalog number IS-7F07, Disposable, Single Use, Do Not Re-sterilize, Manufactured in USA for VNUS, 5799 Fontanus Way, San Jose CA 95138 USA; General: 408-360-7200. For catheter exchange or placement of closed… |
| Product code | DRE |
| Recalling firm | Argon Medical Devices, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 14, 2010 |
| 510(k) numbers | K780126 |
| FEI number | 1625425 |
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