Device recall
Z-0156-2007: DermaStyle Chroma 2-blue and red light device indicated to be used in treating…
FDA device recall · Class II · Lumiport, LLC
Key facts
| Recall number (Z-number) | Z-0156-2007 |
|---|---|
| Recall event | 36406 |
| Product | DermaStyle Chroma 2-blue and red light device indicated to be used in treating skin blemishes; portable home therapy; Lumiport LLC. |
| Product code | MOQ |
| Recalling firm | Lumiport, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2012 |
| FEI number | 3005952043 |
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