Data Foundry

Medical device recalls 2014

Ultraslim — Class II medical device recall Z-2645-2014

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 numberZ-2645-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAdvanced Photonic Systems, LLC, Cocoa Beach, FL, United States
Recall initiated2014-05-06
Classified2014-09-16
Reported by FDA2014-09-24
Terminated2015-06-24
DistributedAL, 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 USCA, CH, FR
Quantity235 total
Model numbersBR-144, BRC-144, BRS-144

Product

Ultraslim. 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 program combines detoxification, red light exposure, hydration, full body vibration, massage, Niacin, Milk Thistle, and the use of compression garments. Sensible diet and exercise are recommended, but not required.

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-2645-2014. 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.