Forever Beautiful INFINITY — Class I drug recall D-0993-2015
Terminated recall by REFA Enterprises, LLC, reported 2015-05-13, distributed nationwide. Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain sibutramine and phenolphthalein
| Recall number | D-0993-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | REFA Enterprises, LLC, Virginia Beach, VA, United States |
| Recall initiated | 2014-11-03 |
| Classified | 2015-05-06 |
| Reported by FDA | 2015-05-13 |
| Terminated | 2015-11-04 |
| Distributed | Nationwide (US) |
| Quantity | 92 bottles |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00633090804649 |
Product
Forever Beautiful INFINITY, capsules, 300mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
Reason for recall
Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain sibutramine and phenolphthalein
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/D-0993-2015. 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.