Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules — Class I drug recall D-1368-2014
Terminated recall by Pure Edge Nutrition, reported 2014-06-18, distributed nationwide. Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein
| Recall number | D-1368-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pure Edge Nutrition, Toms River, NJ, United States |
| Recall initiated | 2013-10-10 |
| Classified | 2014-06-12 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2016-10-07 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen, unapproved product |
| Lot numbers | 2015/07/08, BTRX7654 |
Product
Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules, 30 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
Reason for recall
Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & 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-1368-2014. 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.