Device recall
Z-1638-2008: VECTRA GENISYS, electromechanical therapeutic ultrasound and powered muscle…
FDA device recall · Class II · Chattanooga Corp Inc
Key facts
| Recall number (Z-number) | Z-1638-2008 |
|---|---|
| Recall event | 47428 |
| Product | VECTRA GENISYS, electromechanical therapeutic ultrasound and powered muscle stimulation device, Model No. 2761, Chattanooga Group. |
| Product code | IMG |
| Recalling firm | Chattanooga Corp Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 19, 2010 |
| 510(k) numbers | K031077 |
| FEI number | 1000342033 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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