Device recall
Z-0219-05: Proteus XR/a Radiographic X-ray System, models 2259973-1, 2259973-2, 2259973-3…
FDA device recall · Class II · General Electric Med Systems LLC
Key facts
| Recall number (Z-number) | Z-0219-05 |
|---|---|
| Recall event | 30761 |
| Product | Proteus XR/a Radiographic X-ray System, models 2259973-1, 2259973-2, 2259973-3, 2259973-4. The system consists of a radiographic table, a overhead tube suspension, high frequency generator and power distribution unit, wall stand, dual focal spot x-ray tube and operator''s console. |
| Product code | KPR |
| Recalling firm | General Electric Med Systems LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 21, 2006 |
| 510(k) numbers | K993090 |
| 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