FDA Device recall Z-1538-2013
Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such
- FDA Device
- Class II
- terminated
- Published 2013-09-25
On 2013-09-25 the FDA classified a Class II recall of Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such by Laserworld Usa, citing A potential lack of certification, and/or missing laser certification, laser safety warning and administrative labels, and potentially incomplete Performance Feature set and incom….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1538-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-07-19 |
| Published | 2013-09-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Laserworld Usa |
| Distribution | CA, CO, FL, KS, PA |
Product
Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such.
Reason
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.
Identifiers
| code_info | All projectors distributed between 2008 and 2012, including, but not limited to, the Proline Series AG, Revolution Seri…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1538-2013%22
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