Laserworld RGB & Piko Nano RGB Models All models are laser light show… — Class II medical device recall Z-1538-2013
Terminated recall by Laserworld Usa Inc, reported 2013-09-25, distributed in CA, CO, FL, KS, PA. A potential lack of certification, and/or missing laser certification, laser safety warning and administrative
| Recall number | Z-1538-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Laserworld Usa Inc, New York, NY, United States |
| Recall initiated | 2012-07-19 |
| Classified | 2013-09-19 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2018-06-29 |
| Distributed | CA, CO, FL, KS, PA |
| Reason classes | labeling |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1538-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.