Device recall
Z-0896-06: GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova…
FDA device recall · Class II · GE Healthcare
Key facts
| Recall number (Z-number) | Z-0896-06 |
|---|---|
| Recall event | 34758 |
| Product | GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova 2000S mobile version. Cardiovascular Imaging System. |
| Product code | MQB |
| Recalling firm | GE Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 2008 |
| 510(k) numbers | K022322, K024200 |
| FEI number | 2126677 |
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