Device recall
Z-0200-2009: Monitor suspensions used with Advantx Legacy, RFX Classical, SFX-90, Model #…
FDA device recall · Class II · GE Healthcare
Key facts
| Recall number (Z-number) | Z-0200-2009 |
|---|---|
| Recall event | 49581 |
| Product | Monitor suspensions used with Advantx Legacy, RFX Classical, SFX-90, Model # 46-240838G2, manufactured after March 8, 1985 for Advantx Legacy, RFX and SFX systems. General-purpose radiographic system component used to suspend the system's image monitor. |
| Product code | IZO |
| Recalling firm | GE Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 2012 |
| 510(k) numbers | K760466, K801320, K931049 |
| FEI number | 2126677 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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