Quasar Bio-Tech recalls Pure Rayz Light Therapy System due to unapproved claims about collagen and elastin production. This device was not cleared by the FDA for these health claims.
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
Quasar Bio-Tech is recalling their Pure Rayz Light Therapy System because it was not approved by the FDA for claims about reducing wrinkles through collagen and elastin production. This means the device may not work as advertised for skin health.
The device makes health claims about collagen and elast:in production that the FDA did not approve. This means the device might not work as advertised for skin health, but it does not pose a physical risk like injury or fire.
People who own the Pure Rayz Light Therapy System, especially those using it for skin treatments. Those with medical conditions or sensitive skin may be at slightly higher risk due to unverified claims.
Check for the Pure Rayz Light Therapy System with product number DPA-026 or UPC code 0 91037 46140 7. The device is a handheld wrinkles reduction device sold with packaging, box, sleeve, and user manual.
Look for the product number DPA-026 or UPC code 0 91037 46140 7 on the packaging, box, sleeve, or user manual.
No, the device does not pose a physical risk like injury or fire. The recall is due to unapproved health claims, not a safety hazard.
Quasar Bio-Tech did not receive FDA clearance for claims about collagen and elastin production as stated on the packaging and user manuals.
Check the product number or UPC code to confirm if you have the recalled item. The recall does not require immediate action beyond verifying ownership.
We’ve drafted a message you can send Quasar Bio-Tech to request your refund or repair — edit it as you like.
Subject: Recall Z-2975-2018 — Quasar Bio-Tech Quasar Bio-Tech Hello, I own a Quasar Bio-Tech that is covered by recall Z-2975-2018 from Quasar Bio-Tech. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
