FDAFDA · Food and drugs·Recall number Z-1538-2013
Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such.
Published September 25, 2013 · Recall initiated: July 19, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Laserworld Usa Inc
- Distributor
- US Distribution including the states of CA, CO, FL, KS and PA.
- Lot
- 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
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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