Device recall
Z-1172-06: Voluson 730 Expert, Voluson 730 Pro, Voluson 730 ProV with software versions…
FDA device recall · Class III · General Electric Med. Sys. Ultrasound
Key facts
| Recall number (Z-number) | Z-1172-06 |
|---|---|
| Recall event | 35066 |
| Product | Voluson 730 Expert, Voluson 730 Pro, Voluson 730 ProV with software versions 4.0.0, 4.0.1, 4.0.2, 4.0.3, 4.0.4, 4.0.5, 5.00, 5.0.1. The device is a general-purpose diagnostic ultrasound system. |
| Product code | IYN |
| Recalling firm | General Electric Med. Sys. Ultrasound |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 6, 2007 |
| 510(k) numbers | K041688 |
| FEI number | 1000116747 |
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