Device recall
Z-0306-04: Performix X-ray Tube - Performix ADV, Performix Ultra, Solarix 630.
FDA device recall · Class II · General Electric Med Systems
Key facts
| Recall number (Z-number) | Z-0306-04 |
|---|---|
| Recall event | 27927 |
| Product | Performix X-ray Tube - Performix ADV, Performix Ultra, Solarix 630. |
| Product code | IYB |
| Recalling firm | General Electric Med Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 15, 2005 |
| 510(k) numbers | K013561, K023988 |
| 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