Device recall
Z-0301-2026: Optima NX; dual-head nuclear medicine gamma camera designed specifically for…
FDA device recall · Class II · GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Key facts
| Recall number (Z-number) | Z-0301-2026 |
|---|---|
| Recall event | 97647 |
| Product | Optima NX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging |
| Product code | KPS |
| Recalling firm | GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3027338963 |
At a glance
- None 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