X-Laser Llc: Medical Device Recall in 2017 - (Recall #: Z-2870-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Beam, Hawk 500 High-power laser light show projector.

Product Classification:

Class II

Date Initiated: July 24, 2017

Date Posted: September 20, 2017

Recall Number: Z-2870-2017

Event ID: 77843

Reason for Recall:

Failure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessible auto and music modes of operation

Status: Terminated

Product Quantity: 830

Code Information:

LLS projectors

Distribution Pattern:

US Distribution

Voluntary or Mandated:

FDA Mandated