The Recall Desk
HighFDA (Devices)·Z-2113-2025·Announced 2025-07-23

Laser Light Show Projectors Recalled for Non-Functional Safety Interlock

Beyond Laser Systems is recalling laser light show projectors with missing or non-functional remote safety interlocks that prevent safe shutdown of Class IV lasers. Projectors also lack required labeling and user documentation.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is an FDA Class II recall involving non-functional or missing critical safety interlocks on Class IV laser equipment. While no illnesses or injuries have been reported, this qualifies as a risk-of-harm product where serious injury (eye damage/blindness) is possible. The absence of reported hospitalizations or injuries places it below Severe (4), but the known hazard of Class IV lasers and the missing safety controls warrant High (3) severity.

Plain-English summary

Beyond Laser Systems, LLC is recalling laser light show projectors (Models PURE, CLUB, and DIODE) due to critical defects in safety controls and regulatory compliance. The remote interlock connector, required to safely shutdown the laser during operation, was either not installed or mechanically installed but not wired, rendering the safety system non-functional. The projectors also lack proper labeling required by federal regulation and were shipped without user manuals required for safe operation.

These projectors emit Class IV lasers, the highest hazard class, capable of causing immediate and permanent eye damage from direct or scattered beam exposure. A non-functional or missing safety interlock prevents safe emergency shutdown, creating a serious risk of injury if the equipment is used without proper safety controls.

The recall affects three product families: PURE, CLUB, and DIODE, with various hardware configurations including different port counts and radiant power levels. Consumers who have purchased these projectors should discontinue use immediately and contact Beyond Laser Systems for guidance on repair, replacement, or return.

The recalled product

Product
Laser light show projectors manufactured by BLS, Model PURE 5000/10000.
Manufacturer
Beyond Laser Systems, LLC
Category
Medical Device — Laser Equipment
Hazard
  • laser-exposure
  • missing-safety-interlock
  • inadequate-labeling
  • missing-documentation

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • N/A

Distribution

Distributed nationwide across the United States.

Related recalls

Same category