Dream Body Slimming Capsule — Class I drug recall D-1222-2014
Terminated recall by Slim Beauty USA, reported 2014-04-16, distributed nationwide. Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and . Sibutramine is not cu
| Recall number | D-1222-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Slim Beauty USA, Kearney, NE, United States |
| Recall initiated | 2013-12-10 |
| Classified | 2014-04-07 |
| Reported by FDA | 2014-04-16 |
| Terminated | 2017-03-14 |
| Distributed | Nationwide (US) |
| Quantity | 3 bottles |
| Reason classes | undeclared allergen, unapproved product |
| Lot numbers | 20130328 |
| Expiration dates | 2015-03-27 |
Product
Dream Body Slimming Capsule (Chinese bitter orange 24%, Cassia Seed 18%, Aloe 16%, Lotus Leaf Extract 12%, Medical Amylum 30%), 350 mg, 30-count bottles, Made in China (Beijing).
Reason for recall
Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and . Sibutramine is not currently marketed in the United States, making this product an unapproved new drug.
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-1222-2014. 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.