FDAFDA · Food and drugs·Recall number Z-2975-2018
Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
Published September 12, 2018 · Recall initiated: June 29, 2018
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
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Quasar Bio-Tech, Inc.
- Distributor
- Nationwide distribution to CA, FL, GA, HI, IL, LA, MD, NE, NY, OH, TX, VA, WA, WI. Worldwide distribution to Australia, China, Netherlands, United Kingdom
- Lot
- Product Number DPA-026. UPC Code 0 91037 46140 7
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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