Z-1538-2013 Class II Terminated
FDA device recall Z-1538-2013 was initiated by Laserworld Usa Inc on July 19, 2012 and is designated Class II. 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 Informatio… The recall status is terminated (terminated June 29, 2018). Affected quantity: Total distribution of more than 500 units between July1, 2008, and June 30, 2012.
Recall Details
- Product Type
- Devices
- Report Date
- September 25, 2013
- Initiation Date
- July 19, 2012
- Termination Date
- June 29, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- Total distribution of more than 500 units between July1, 2008, and June 30, 2012
Product Description
Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such.
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.
Distribution Pattern
US Distribution including the states of CA, CO, FL, KS and PA.
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