FDAJune 29, 2018device
Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
Official recall recorded by the U.S. Food & Drug Administration.
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
FDA enforcement status: Terminated
Brands named
quasar bio techquasarquasar bio
UPCs
091037461407
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCJunpower CR2032 Lithium Coin Batteries Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Federal Statute for Child-Resistant Packaging of Coin Batteries; Sold on Amazon by JSNJ_Tech Store2026-07-02
- CPSCArizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by 7111495 Canada2026-06-18
- CPSCWagner Spray Tech Recalls 900 Series Power Steamers Due to Burn Hazard2026-03-19
- CPSCEvajoy Above-Ground Pools 48 Inches and Taller Recalled Due to Drowning Hazard; Manufactured by Shenzhen Danya Tech2026-02-26
- CPSCJohnson Health Tech Expands Recall to Include Matrix Retail and Vision Treadmills Due to Fire Hazard2026-01-22
- FDAThe Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips; URIMED Urinalysis Reagent Strips URS-5, Rapid UTI Test Includes Ketones: Leukocytes, Nitrite, pH, Ketone, Protein; Vivoo Ketone Test2025-11-22
- FDAMenopause Test Cassette (Urine)2025-11-22
- FDAS. Typhi/Para Typhi A Antigen2025-11-22
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