Device recall
Z-1088-2007: GE Innova 2100-IQ Digital Fluoroscopic Imaging System, Versatile cardiac and…
FDA device recall · Class II · GE Healthcare
Key facts
| Recall number (Z-number) | Z-1088-2007 |
|---|---|
| Recall event | 44936 |
| Product | GE Innova 2100-IQ Digital Fluoroscopic Imaging System, Versatile cardiac and vascular imaging system. GE Healthcare Americas P.O.Box 414, Milwaukee, Wisconsin 53201, U.S.A. |
| Product code | MQB |
| Recalling firm | GE Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 8, 2015 |
| 510(k) numbers | K050489 |
| 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