Device recall
Z-1600-2009: GE Healthcare CIC Pro Clinical Information Center Central Station (CIC Pro…
FDA device recall · Class II · GE Medical Systems Information Tecnology
Key facts
| Recall number (Z-number) | Z-1600-2009 |
|---|---|
| Recall event | 52002 |
| Product | GE Healthcare CIC Pro Clinical Information Center Central Station (CIC Pro version 5.1, MP100 Hardware). The CIC Pro" clinical Information Center central station is intended to collect information from a network and display this date. This data includes physiological, patient dermographic and/or… |
| Product code | DSI |
| Recalling firm | GE Medical Systems Information Tecnology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 16, 2012 |
| 510(k) numbers | K062976 |
| FEI number | 3005860720 |
At a glance
- 1–9 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