Recall Z-1538-2013— Laserworld Usa Inc
Class II · Terminated
Class II FDA medical device recall by Laserworld Usa Inc, initiated 2012-07-19, terminated 2018-06-29. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Laserworld Usa Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2012-07-19
- Terminated
- 2018-06-29
- Firm location
- New York, NY, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.