Quasar Bio-Tech, Inc. recalls Quasar MD Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.

Recalled September 12, 2018 · FDA recall Z-2974-2018 · Quasar Bio-Tech

Hazard

Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals. · FDA Class II

Units

6,783 units total

Sold at

Nationwide distribution to CA, FL, GA, HI, IL, LA, MD, NE, NY, OH, TX, VA, WA, WI. Worldwide distribution to Australia, China, Netherlands, United Kingdom

Description

Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.

Product

Quasar MD Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.

Manufacturer(s)

Quasar Bio-Tech, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →