Device recall
Z-1192-2012: Visionsense Stereoscopic Vision System, Brand name VSII, Model/Part Numbers…
FDA device recall · Class II · Visionsense, Ltd.
Key facts
| Recall number (Z-number) | Z-1192-2012 |
|---|---|
| Recall event | 61279 |
| Product | Visionsense Stereoscopic Vision System, Brand name VSII, Model/Part Numbers 172-0030 and 172-0040 --- Classification Name: Neurological Endoscope --- NOTE: Model Numbers 172-0032, 172-0044, 172-0070, 172-0072, 172-0080 were also included in the firm's recall action but these never entered US… |
| Product code | GWG |
| Recalling firm | Visionsense, Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2012 |
| 510(k) numbers | K081102 |
| FEI number | 3003143838 |
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