Device recall
Z-2349-2010: Picasso/Picasso Lite lasers Intended use: Dentistry.
FDA device recall · Class II · AMD Lasers, LLC
Key facts
| Recall number (Z-number) | Z-2349-2010 |
|---|---|
| Recall event | 56330 |
| Product | Picasso/Picasso Lite lasers Intended use: Dentistry. |
| Product code | GEX |
| Recalling firm | AMD Lasers, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 21, 2011 |
| FEI number | 3003258642 |
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