Device recall
Z-0506-2007: The LightSpeed RT16 CT Scanner System is indicated for head and whole body X-ray…
FDA device recall · Class II · GE Healthcare
Key facts
| Recall number (Z-number) | Z-0506-2007 |
|---|---|
| Recall event | 37028 |
| Product | The LightSpeed RT16 CT Scanner System is indicated for head and whole body X-ray Computed Tomography applications. The system is capable of generating images for the guidance of minimally invasive procedures such as biopsy and ablation of tumors and pathology. The system allows imaging of obese… |
| Product code | JAK |
| Recalling firm | GE Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 30, 2007 |
| 510(k) numbers | K060052 |
| 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