Quasar Bio-Tech recalls Baby Quasar Plus Light Therapy System due to unapproved collagen and elastin claims on packaging and manuals. No FDA clearance was received 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 Baby Quasar Plus Light Therapy System because it was sold with unapproved health claims about collagen and elast: the product was not cleared by the FDA for these claims. This means the device may mislead users about its benefits.
The device was sold with packaging and manuals claiming to produce collagen and elastin, but Quasar did not get FDA approval for these health claims. This means the product may not work as advertised for skin care.
Parents or caregivers who purchased the Baby Quasar Plus Light Therapy System for skin care. Children using the device are at risk of being misled about its health benefits.
Check for the product name 'Baby Quasar Plus Light Therapy System' on packaging, box, sleeve, or user manual. The product number is DPA-023 and UPC code is 0 91037 46144 5.
Look for the product name 'Baby Quasar Plus Light Therapy System' on packaging, box, sleeve, or user manual.
Quasar did not receive FDA clearance for claims of collagen and elastin production as stated on the packaging and in the user manuals.
The recall record does not specify a remedy, so check the product details and contact Quasar Bio-Tech for further instructions.
The recall is due to unapproved health claims, not a physical hazard. There is no risk of injury mentioned in the record.
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-2973-2018 — Quasar Bio-Tech Quasar Bio-Tech Hello, I own a Quasar Bio-Tech that is covered by recall Z-2973-2018 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.
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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.
