Quasar Bio-Tech Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual recall — FDA Z-2975-2018
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
Overview of recall records associated with Quasar Bio-Tech, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 3.
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
This page summarizes recall records in which the official source identifies Quasar Bio-Tech, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.