Device recall
Z-2040-2012: OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during…
FDA device recall · Class I · GE OEC Medical Systems, Inc
Key facts
| Recall number (Z-number) | Z-2040-2012 |
|---|---|
| Recall event | 62382 |
| Product | OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device… |
| Product code | OXO |
| Recalling firm | GE OEC Medical Systems, Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 13, 2013 |
| 510(k) numbers | K992506 |
| FEI number | 1720753 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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