Device recall
Z-0870-2009: Centricity Enterprise Web 3.0 software; the software allows physicians…
FDA device recall · Class II · GE Healthcare Integrated IT Solutions
Key facts
| Recall number (Z-number) | Z-0870-2009 |
|---|---|
| Recall event | 50540 |
| Product | Centricity Enterprise Web 3.0 software; the software allows physicians convenient, quick access to medical images and related data they need via a web browser, password and a standard PC; GE Healthcare Integrated IT Solutions, Barrington, IL 60010. |
| Product code | LMD |
| Recalling firm | GE Healthcare Integrated IT Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 18, 2010 |
| FEI number | 3004526608 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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