# FDA recall Z-2974-2018

> **Quasar Bio-Tech, Inc.** · Class II · device recall initiated 2018-06-29.

## Product

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

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-2974-2018
- **Recalling firm:** Quasar Bio-Tech, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-06-29
- **Report date:** 2018-09-12
- **Termination date:** 2019-08-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sarasota, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2974-2018

## Citation

> AI Analytics. FDA recall Z-2974-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2974-2018. Source: US FDA. Licensed CC0.

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