Quasar Bio-Tech, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2974-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 29, 2018

Date Posted: September 12, 2018

Recall Number: Z-2974-2018

Event ID: 80496

Reason for Recall:

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

Status: Terminated

Product Quantity: 6,783 units total

Code Information:

Product Number DPA-024. UPC Code 0 91037 46143 8

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated