Burn 7 Capsules — Class I drug recall D-1351-2014
Terminated recall by Deseo Rebajar, reported 2014-06-04, distributed in PR. Marketed Without an Approved NDA/ANDA: Undeclared sibutramine and phenolphthalein in Burn 7 dietary supplement
| Recall number | D-1351-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Deseo Rebajar, Fajardo, PR, United States |
| Recall initiated | 2013-12-23 |
| Classified | 2014-05-27 |
| Reported by FDA | 2014-06-04 |
| Terminated | 2017-05-03 |
| Distributed | PR |
| Quantity | 120 bottles |
| Reason classes | undeclared allergen, unapproved product |
| Expiration dates | 2015-07-17 |
Product
Burn 7 Capsules, supplied in 30 capsules bottle
Reason for recall
Marketed Without an Approved NDA/ANDA: Undeclared sibutramine and phenolphthalein in Burn 7 dietary supplement
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-1351-2014. 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.