Device recall
Z-3170-2026: Workflow Core Services V8, intended to provide set of services for storage and…
FDA device recall · Class II · GE Healthcare
Key facts
| Recall number (Z-number) | Z-3170-2026 |
|---|---|
| Recall event | 99661 |
| Product | Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administration, common configuration management for consuming applications, 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