Device recall
Z-0768-2020: LightPod ERA lasers
FDA device recall · Class II · Aerolase Corporation
Key facts
| Recall number (Z-number) | Z-0768-2020 |
|---|---|
| Recall event | 84568 |
| Product | LightPod ERA lasers |
| Product code | GEX |
| Recalling firm | Aerolase Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 30, 2021 |
| FEI number | 3004374705 |
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