Vy&Tea — Class I drug recall D-0749-2021
Ongoing recall by Qikmoov LLC, reported 2021-08-11, distributed nationwide. Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine.
| Recall number | D-0749-2021 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Qikmoov LLC, Norwalk, CA, United States |
| Recall initiated | 2021-07-14 |
| Classified | 2021-08-17 |
| Reported by FDA | 2021-08-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CA, CH, DE, FR, GB, HK, IT, SE, TH |
| Quantity | 591 boxes |
| Reason classes | unapproved product |
| Expiration dates | 2021-09 |
Product
Vy&Tea (Vietnamese Labeling with a green leaf and a bird underneath) 15/KLT 45.0G (15 tea sachets per box), Manufactured by Havyco No. 45, Group 1, National Highway 14, Son Hiep Hamlet, Tho Son Commune, Bu Dang District, Binh Phuoc Province, Vietnam, Website: trathaomocgiamcan.com.
Reason for recall
Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine.
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-0749-2021. 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.