Drug recall
Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.
FDA recall event 97176 · Class II · Beyond Laser Systems, LLC
Key facts
| Event ID | 97176 |
|---|---|
| Recall numbers | Z-2111-2025, Z-2112-2025, Z-2113-2025 |
| Recalling firm | Beyond Laser Systems, LLC |
| Product type | Devices |
| Products | Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000., Laser light show projectors manufactured by BLS, Model DIODE 1000/2000/3000., Laser light show projectors manufactured by BLS, Model PURE 5000/10000. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA Requested |
| Reason for recall | The remote interlock connector, which is required by 21 CFR 1040.10(f)(3), in the remote stop box was not installed the connector or was mechanically installed but not wired. The labels placed on the… |
| Initiation date | Jun 30, 2025 |
| Report date | Jul 23, 2025 |
| City | Austin |
| State | TX |
| Country | United States |
| FEI number | 3021802180 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: