Device recall
Z-0101-04: Vari-Lase Endovenous Laser Procedural Kit, Model 7000
FDA device recall · Class II · Vascular Solutions, Inc
Key facts
| Recall number (Z-number) | Z-0101-04 |
|---|---|
| Recall event | 27557 |
| Product | Vari-Lase Endovenous Laser Procedural Kit, Model 7000 |
| Product code | GEX |
| Recalling firm | Vascular Solutions, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 2005 |
| 510(k) numbers | K030654 |
| FEI number | 3002827704 |
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