Device recall
Z-2839-2011: Therakos Cellex Procedural Kits. Designed to interface with the Cellex…
FDA device recall · Class II · Therakos Inc
Key facts
| Recall number (Z-number) | Z-2839-2011 |
|---|---|
| Recall event | 57518 |
| Product | Therakos Cellex Procedural Kits. Designed to interface with the Cellex Photopheresis System to perform cell separation and photoactivation in a single, closed and sterile circuit. |
| Product code | LNR |
| Recalling firm | Therakos Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 19, 2015 |
| 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