Device recall
Z-2600-2011: Prism Laser 7642 Laser System
FDA device recall · Class II · American Stress Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-2600-2011 |
|---|---|
| Recall event | 58804 |
| Product | Prism Laser 7642 Laser System |
| Product code | REO |
| Recalling firm | American Stress Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2016 |
| FEI number | 3008905686 |
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