Device recall
Z-3171-2026: Core Services Hub V8, a set of backend services including Cross Enterprise (XE)…
FDA device recall · Class II · GE Healthcare
Key facts
| Recall number (Z-number) | Z-3171-2026 |
|---|---|
| Recall event | 99661 |
| Product | Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise imaging workflows, All versions |
| Product code | LLZ |
| Recalling firm | GE Healthcare |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K043415, K110875 |
| FEI number | 3004526608 |
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