Device recall
Z-1783-2024: GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems
FDA device recall · Class II · GE Medical Systems, SCS
Key facts
| Recall number (Z-number) | Z-1783-2024 |
|---|---|
| Recall event | 94305 |
| Product | GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems |
| Product code | OWB |
| Recalling firm | GE Medical Systems, SCS |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K181403 |
| FEI number | 1000284313 |
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