Device recall
Z-1280-2012: VeinViewer (R) by Luminetx, Model Number VV1.0, Part No: P00399-L, Luminetx…
FDA device recall · Class II · Christie Medical Holding Inc
Key facts
| Recall number (Z-number) | Z-1280-2012 |
|---|---|
| Recall event | 61420 |
| Product | VeinViewer (R) by Luminetx, Model Number VV1.0, Part No: P00399-L, Luminetx Corporation, Memphis, TN 38104 Product Usage: Non- invasive electronic visual aid device designed to project an image of a superficial subcutaneous vascular structures on the surface of the skin |
| Product code | KZA |
| Recalling firm | Christie Medical Holding Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 23, 2012 |
| FEI number | 3008161930 |
At a glance
- None 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