Device recall
Z-0939-2011: Linemaster Wireless Footswitch, VASER System, REF Vaser 2.0, Sound Surgical…
FDA device recall · Class II · Sound Surgical Technologies, LLC
Key facts
| Recall number (Z-number) | Z-0939-2011 |
|---|---|
| Recall event | 57630 |
| Product | Linemaster Wireless Footswitch, VASER System, REF Vaser 2.0, Sound Surgical Technologies LLC, 357 South McCaslin Blvd., Suite 100, Louisville, CO 80027 |
| Product code | GEI |
| Recalling firm | Sound Surgical Technologies, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 8, 2011 |
| 510(k) numbers | K022051, K991791, K993868 |
| FEI number | 3004106598 |
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