Laser Light Show Projectors Recalled for Missing Safety Interlocks and Labels
Beyond Laser Systems is recalling laser light show projectors for missing safety interlocks and required labels. Affected models lack the remote interlock connector needed to prevent user exposure to Class IV laser radiation.
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 a risk-of-harm product involving Class IV lasers with missing safety interlocks and required safety labels. Although no injuries have been reported, the defects create a serious risk of laser exposure to users, particularly the missing remote interlock connector that is required to prevent laser emission during unsafe conditions.
Plain-English summary
Beyond Laser Systems, LLC is recalling laser light show projectors (Models CLUB 1000/2000/4000). These projectors use Class IV lasers and have been distributed throughout the United States. Approximately 12 units have been identified in this recall.
The recalled projectors have serious safety defects. The remote interlock connector, which is required to shut down the laser when the projector is accessed or moved, was either not installed or was mechanically installed but not wired. Additionally, the projectors lack required safety labels and identification markings, and no user manuals were provided to explain safe operation. The projectors also failed quality control testing of the manual reset function.
Class IV lasers can cause serious eye damage and injury. Without the remote interlock connector and proper safety labels and instructions, users may be exposed to harmful laser radiation. The missing interlock is particularly critical because it prevents the laser from shutting down during unsafe situations.
If you own one of these projectors, do not use it. Contact Beyond Laser Systems for corrective repairs or return instructions. Do not operate the projector until the safety defects have been corrected.
The recalled product
- Product
- Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.
- Manufacturer
- Beyond Laser Systems, LLC
- Hazard
- laser-exposure
- missing-interlock
- missing-labels
- missing-manuals
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
- CriticalMedline spinal anesthetic kits recalled for quality and efficacy concerns
FDA (Devices) · 2026-06-03
- SevereMedline Spinal Trays Recalled Due to Quality and Efficacy Concerns
FDA (Devices) · 2026-06-03
- SevereMedline Spinal Block Kits Recalled for Data Integrity and Efficacy Issues
FDA (Devices) · 2026-06-03
- HighMedline Medical Convenience Kit Recalled: Wrong Syringe Type Inside
FDA (Devices) · 2026-06-03
- SevereMedline spinal anesthesia kits recalled for bupivacaine quality issues
FDA (Devices) · 2026-06-03