Device recall
Z-2067-2011: Therakos UVAR XTS Procedural Kits Is indicated for use in the ultraviolet-A…
FDA device recall · Class II · Therakos Inc
Key facts
| Recall number (Z-number) | Z-2067-2011 |
|---|---|
| Recall event | 57912 |
| Product | Therakos UVAR XTS Procedural Kits Is indicated for use in the ultraviolet-A (UVA) irradiation. |
| Product code | LNR |
| Recalling firm | Therakos Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2014 |
| PMA numbers | P860003 |
| FEI number | 2523595 |
At a glance
- None 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