Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules — Class I drug recall D-1370-2014
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-1370-2014 |
|---|---|
| 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 | 2015/05/20, 2015/08/12, AU2013AB, BVAU813 |
Product
Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules, 60 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-1370-2014. 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.