Device recall
Z-1966-2015: GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and…
FDA device recall · Class II · GE Healthcare
Key facts
| Recall number (Z-number) | Z-1966-2015 |
|---|---|
| Recall event | 71572 |
| Product | GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and Fluoroscopic Systems. A universal diagnostic imaging system for radiographic and fluoroscopic examinations. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position. Legacy and… |
| Product code | JAA |
| Recalling firm | GE Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2015 |
| 510(k) numbers | K081091, K973039 |
| FEI number | 2126677 |
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