Photonica Light Modulator — Class II medical device recall Z-2647-2014
Terminated recall by Advanced Photonic Systems, LLC, reported 2014-09-24, distributed in AL, AZ, CA, CO, FL, GA, ID, IL…. Marketing without marketing clearance or approval.
| Recall number | Z-2647-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Photonic Systems, LLC, Cocoa Beach, FL, United States |
| Recall initiated | 2014-05-06 |
| Classified | 2014-09-16 |
| Reported by FDA | 2014-09-24 |
| Terminated | 2015-06-24 |
| Distributed | AL, AZ, CA, CO, FL, GA, ID, IL, IN, LA, MA, MD, MI, MN, MO, NC, NJ, NV, NY, OH, PA, TX, UT, VA |
| Countries outside the US | CA, CH, FR |
| Quantity | 235 total |
| Model numbers | TDR-1, TDR-2, ULT-1 |
Product
Photonica Light Modulator. These include all products labeled as UltraSlim, Luxurian, BioSlim Lipo, Cellulize, Slim 'n Trim, UltraRed, UltraBlue, Slim-PRO, Dazzle Light, UltraSlim Cold Light, SlenderRay, and U-Slim It, as well as those products with private labelling branding. Company claims that the product provide non-invasive solutions to improve the appearance of fat accumulations, cellulite, fine lines, wrinkles, skin tone, and blemishes.
Reason for recall
Marketing without marketing clearance or approval.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2647-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.