Device recall
Z-1155-2008: GE LOGIQ 3 Expert ultrasound scanner with software versions 4.0.5, 4.1.1 and…
FDA device recall · Class II · GE Healthcare Clinical Systems
Key facts
| Recall number (Z-number) | Z-1155-2008 |
|---|---|
| Recall event | 44884 |
| Product | GE LOGIQ 3 Expert ultrasound scanner with software versions 4.0.5, 4.1.1 and 4.1.2. GE Healthcare P.O. Box 414, Milwaukee, Wisconsin 53201 |
| Product code | IYN |
| Recalling firm | GE Healthcare Clinical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 29, 2012 |
| 510(k) numbers | K020263 |
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