Device recall
Z-1232-2009: GE Healthcare CIC Pro" Software Versions 5.0.3, 5.0.6,5.0.7, 5.0.8 and 4.1. The…
FDA device recall · Class II · GE Medical Systems Information Tecnology
Key facts
| Recall number (Z-number) | Z-1232-2009 |
|---|---|
| Recall event | 51253 |
| Product | GE Healthcare CIC Pro" Software Versions 5.0.3, 5.0.6 ,5.0.7, 5.0.8 and 4.1. The CIC Pro" Clinical Information Center Central Station is intended for use under the direct supervision of a licensed healthcare practitioner. The intended use is to provide clinicians with adult, pediatric and neonatal… |
| Product code | DSI |
| Recalling firm | GE Medical Systems Information Tecnology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 15, 2014 |
| 510(k) numbers | K032370, K053356, 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