Skinny Bee Diet capsules — Class I drug recall D-0223-2017
Terminated recall by Love My Tru Body, reported 2016-12-28, distributed nationwide. Marketed without an approved NDA/ANDA: presence of undeclared sibutramine, desmethylsibutramine (an active met
| Recall number | D-0223-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Love My Tru Body, McDonough, GA, United States |
| Recall initiated | 2016-10-28 |
| Classified | 2016-12-22 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2017-04-06 |
| Distributed | Nationwide (US) |
| Quantity | 74 bottles |
| Reason classes | undeclared allergen, unapproved product |
| Expiration dates | 2018-03-06 |
Product
Skinny Bee Diet capsules, 500 mg, packaged in a 60-count bottle
Reason for recall
Marketed without an approved NDA/ANDA: presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of 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-0223-2017. 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.