Device recall
Z-2113-2025: Laser light show projectors manufactured by BLS, Model PURE 5000/10000.
FDA device recall · Class II · Beyond Laser Systems, LLC
Key facts
| Recall number (Z-number) | Z-2113-2025 |
|---|---|
| Recall event | 97176 |
| Product | Laser light show projectors manufactured by BLS, Model PURE 5000/10000. |
| Product code | REA |
| Recalling firm | Beyond Laser Systems, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3021802180 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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