Vail-Bon Jie Yang Wan capsules — Class I drug recall D-0008-2025
Ongoing recall by 123Herbals, reported 2024-10-16. Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorphen
| Recall number | D-0008-2025 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | 123Herbals, Rosemead, CA, United States |
| Recall initiated | 2024-09-18 |
| Classified | 2024-10-10 |
| Reported by FDA | 2024-10-16 |
| Reason classes | undeclared allergen, unapproved product |
Product
Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn. Bhd., No 1, Lorong Mengkudu, Taman Mengkudu, 14100 Juru, Malaysia.
Reason for recall
Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.
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-0008-2025. 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.