FDA Device recall Z-2975-2018
Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual
- FDA Device
- Class II
- terminated
- Published 2018-09-12
On 2018-09-12 the FDA classified a Class II recall of Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual by Quasar Bio Tech, citing quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2975-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-29 |
| Published | 2018-09-12 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Quasar Bio Tech |
| Distribution | US |
Product
Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
Reason
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.
Identifiers
| upc | 091037461407 |
|---|---|
| code_info | Product Number DPA-026. UPC Code 0 91037 46140 7 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2975-2018%22
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