Device recall
Z-2873-2018: GE Healthcare Optima CT660. The systems are intended for head, whole body…
FDA device recall · Class II · GE Healthcare Japan Corporation
Key facts
| Recall number (Z-number) | Z-2873-2018 |
|---|---|
| Recall event | 80563 |
| Product | GE Healthcare Optima CT660. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold only outside the U.S. under the following product names: CT OPTIMA 660, CT OPTIMA 660 LONG BJG SKD RUS, CT OPTIMA 660 LONG BJG SKD RUSSIA, CT OPTIMA 660 MID… |
| Product code | JAK |
| Recalling firm | GE Healthcare Japan Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 21, 2020 |
| 510(k) numbers | K082816, K110227, K131576 |
| FEI number | 3002808529 |
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