Device recall
Z-0976-2007: Diamond Mammographic X-Ray System, type MGX-2000, model 5111771. GE Healthcare…
FDA device recall · Class II · General Electric Med Systems LLC
Key facts
| Recall number (Z-number) | Z-0976-2007 |
|---|---|
| Recall event | 37651 |
| Product | Diamond Mammographic X-Ray System, type MGX-2000, model 5111771. GE Healthcare P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A. |
| Product code | IZH |
| Recalling firm | General Electric Med Systems LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 2008 |
| 510(k) numbers | K000976 |
| FEI number | 2126677 |
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