Quasar Bio-Tech recalls handheld wrinkles reduction device due to unapproved collagen/elastin claims on packaging and manuals. No FDA clearance 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 MD Plus Light Therapy System because it makes health claims about collagen and elastin production that the FDA did not approve. This device is marketed as a handheld wrinkles reduction tool but lacks proper regulatory clearance for those specific health benefits.
The device makes health claims about producing collagen and elast:in that the FDA has not approved. This means the device does not have the necessary regulatory clearance to make those specific health claims about skin treatment.
Users of the Quasar MD Plus Light Therapy System who purchased it with the unapproved packaging and manuals are affected. People using the device for skin treatments may be at risk if they believe it provides collagen or elastin benefits.
Check for the product number DPA-024 or UPC code 0 91037 46143 8 on the packaging, box, sleeve, or user manual. The device is marketed as a handheld wrinkles reduction tool.
Look for product number DPA-024 or UPC code 0 91037 46143 8 on packaging, box, sleeve, or user manual.
The device makes health claims about collagen and elastin production that the FDA did not approve.
Check for product number DPA-024 or UPC code 0 91037 46143 8 on packaging, box, sleeve, or user manual. The recall does not require immediate action beyond checking if you have the specific product.
The recall is due to unapproved health claims, not a physical hazard. There is no risk of injury from the device itself.
We’ve drafted a message you can send Quasar to request your refund or repair — edit it as you like.
Subject: Recall Z-2974-2018 — Quasar Quasar Hello, I own a Quasar that is covered by recall Z-2974-2018 from Quasar. 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.
