A1 Slim — Class II drug recall D-0058-2018
Terminated recall by Kiriko, LLC., reported 2017-11-08, distributed nationwide. Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sibutramine, phen
| Recall number | D-0058-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Kiriko, LLC., Manvel, TX, United States |
| Recall initiated | 2017-10-06 |
| Classified | 2017-11-01 |
| Reported by FDA | 2017-11-08 |
| Terminated | 2020-09-09 |
| Distributed | Nationwide (US) |
| Quantity | 700 bottles |
| Reason classes | undeclared allergen, unapproved product |
Product
A1 Slim, Dietary Supplement Beautifully Slim, capsule, 350 mg, 30-count bottle, A1 Slim LLC Pearland TX 77584, www.A1SLIM.COM, info@a1slim.com Bar-Code A105212014
Reason for recall
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine, making this an unapproved drug for which safety and efficacy have not been established and therefore, subject to recall.
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-0058-2018. 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.