The Recall Desk
HighFDA (Devices)·Z-2111-2025·Announced 2025-07-23

BLS DIODE laser projectors shipped without a working remote interlock connector

BLS laser light show projectors, models DIODE 1000, 2000 and 3000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 10 units affected.

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: Risk-of-harm product: a required laser safety interlock was absent or unwired, with no injury reported in the source.

Plain-English summary

Laser light show projectors manufactured by BLS, models DIODE 1000, DIODE 2000 and DIODE 3000, are being recalled. The action covers 10 units.

According to the notice, the remote interlock connector required by 21 CFR 1040.10(f)(3) in the remote stop box was either not installed or was mechanically installed but not wired. The notice also states that the labels placed on the projectors do not meet the requirements of 21 CFR 1010.2, 1010.3, 1010.4 and 1040.10(g), and that the identification label does not include the date of manufacture as required by 21 CFR 1010.3. The FDA classified the action as Class II.

Distribution was nationwide in the United States.

Operators should identify affected projectors by model and follow the instructions issued by the manufacturer.

The recalled product

Product
Laser light show projectors manufactured by BLS, Model DIODE 1000/2000/3000.
Manufacturer
Beyond Laser Systems, LLC
Category
Other — Laser light show projector
Hazard
  • missing-interlock
  • laser-safety
  • labeling-noncompliance
  • class-ii

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