Device recall
Z-1691-2009: GE Innova 4100-IQ, GE Healthcare, Waukesha, WI 53188 ( The system consists of an…
FDA device recall · Class II · Ge Healthcare
Key facts
| Recall number (Z-number) | Z-1691-2009 |
|---|---|
| Recall event | 53260 |
| Product | GE Innova 4100-IQ, GE Healthcare, Waukesha, WI 53188 ( The system consists of an a monoplane positioner, a vascular or cardiac table, an X-ray system and a digital detector). Indicated for use in generating fluoroscopic images of human anatomy for vascular angiography diagnostic and interventional… |
| Product code | MQB |
| Recalling firm | Ge Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2012 |
| 510(k) numbers | K023178, K052412, K061163 |
| FEI number | 3005860720 |
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