Device recall
Z-2184-2017: GE Healthcare Optima CT580; Discovery RT, CT590 RT X-ray system
FDA device recall · Class II · GE Healthcare, LLC
Key facts
| Recall number (Z-number) | Z-2184-2017 |
|---|---|
| Recall event | 77377 |
| Product | GE Healthcare Optima CT580; Discovery RT, CT590 RT X-ray system |
| Product code | JAK |
| Recalling firm | GE Healthcare, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 29, 2018 |
| 510(k) numbers | K093581, K132410 |
| FEI number | 2126677 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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