Device recall
Z-0105-06: Sopha Medical Vision DST / DST-XL Digital vatiable angle Nuclear Imaging System
FDA device recall · Class II · General Electric Med Systems LLC
Key facts
| Recall number (Z-number) | Z-0105-06 |
|---|---|
| Recall event | 33832 |
| Product | Sopha Medical Vision DST / DST-XL Digital vatiable angle Nuclear Imaging System |
| Product code | KPS |
| Recalling firm | General Electric Med Systems LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 26, 2006 |
| 510(k) numbers | K942837 |
| FEI number | 2126677 |
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