Device recall
Z-1519-2015: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options.
FDA device recall · Class II · Lumenis Limited
Key facts
| Recall number (Z-number) | Z-1519-2015 |
|---|---|
| Recall event | 70863 |
| Product | Light Sheer Desire Diode Laser System with XC Handpiece Accessory options. |
| Product code | GEX |
| Recalling firm | Lumenis Limited |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 15, 2016 |
| 510(k) numbers | K003614 |
| FEI number | 3004135191 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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