Laserworld Usa Inc: Medical Device Recall in 2013 - (Recall #: Z-1538-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such.

Product Classification:

Class II

Date Initiated: July 19, 2012

Date Posted: September 25, 2013

Recall Number: Z-1538-2013

Event ID: 62624

Reason for Recall:

A potential lack of certification, and/or missing laser certification, laser safety warning and administrative labels, and potentially incomplete Performance Feature set and incomplete User Information were discovered.

Status: Terminated

Product Quantity: Total distribution of more than 500 units between July1, 2008, and June 30, 2012

Code Information:

All projectors distributed between 2008 and 2012, including, but not limited to, the Proline Series AG, Revolution Series AG, Club Series AG, Clus Series, Pure Light Series, and Revolution Series AG

Distribution Pattern:

US Distribution including the states of CA, CO, FL, KS and PA.

Voluntary or Mandated:

Voluntary: Firm initiated