Device recall
Z-1397-2009: Centricity TriWin Laboratory Information System; GE Healthcare Integrated IT…
FDA device recall · Class II · GE Healthcare Integrated IT Solutions
Key facts
| Recall number (Z-number) | Z-1397-2009 |
|---|---|
| Recall event | 50201 |
| Product | Centricity TriWin Laboratory Information System; GE Healthcare Integrated IT Solutions, Barrington, IL 60010 The Centricity TriWin Laboratory product is a laboratory information system. It is designed to facilitate the general clinical, anatomic pathology, and cytology laboratory workflow such as… |
| Product code | JQP |
| Recalling firm | GE Healthcare Integrated IT Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 11, 2010 |
| FEI number | 3004526608 |
At a glance
- None 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