Device recall
Z-0005-2010: GE OEC 9900 Elite GSP Fluoroscopes To produce mobile fluoroscopic images of…
FDA device recall · Class II · Ge Healthcare
Key facts
| Recall number (Z-number) | Z-0005-2010 |
|---|---|
| Recall event | 53491 |
| Product | GE OEC 9900 Elite GSP Fluoroscopes To produce mobile fluoroscopic images of human anatomy. |
| Product code | JAA |
| Recalling firm | Ge Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 23, 2012 |
| FEI number | 1720753 |
At a glance
- None 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