Device recall
Z-0510-2007: Candela Corporation Vbeam Platinum Laser System, Model/Catalog # 9914-00-0310…
FDA device recall · Class II · Candela Laser Corporation
Key facts
| Recall number (Z-number) | Z-0510-2007 |
|---|---|
| Recall event | 37180 |
| Product | Candela Corporation Vbeam Platinum Laser System, Model/Catalog # 9914-00-0310 Vbeam Platinum w/ rose gray enclosure and rose colored display |
| Product code | GEX |
| Recalling firm | Candela Laser Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 3, 2014 |
| FEI number | 1218402 |
At a glance
- None 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