Device recall
Z-1654-2010: Therakos CellEx Photopheresis System; Photopheresis Procedural Kits, for use…
FDA device recall · Class II · Therakos Inc
Key facts
| Recall number (Z-number) | Z-1654-2010 |
|---|---|
| Recall event | 55300 |
| Product | Therakos CellEx Photopheresis System; Photopheresis Procedural Kits, for use with the THERAKOS CellEx Instrument; |
| Product code | LNR |
| Recalling firm | Therakos Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 2013 |
| 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