Medical device recalls Moderate risk

X-Laser Llc recalls X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Be…

Recall date
July 24, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2870-2017
FDA classification
Class II
Brand / firm
X-Laser Llc
Sold / distributed
US Distribution

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.

Get recall alerts

Free email alert whenever X-Laser Llc has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: X-Laser Llc