FDAClass IISeptember 25, 2013

Laserworld RGB & Piko Nano RGB recall

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

Why was Laserworld RGB & Piko Nano RGB recalled?

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.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such.
Recalling firm
Laserworld Usa Inc
Quantity
Total distribution of more than 500 units between July1, 2008, and June 30, 2012
Distribution
US Distribution including the states of CA, CO, FL, KS and PA.
Recall date
September 25, 2013
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls