FDA Drug recall D-0008-2025
Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn
- FDA Drug
- Class I
- ongoing
- Published 2024-10-16
On 2024-10-16 the FDA classified a Class I recall of Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn by 123herbals, citing marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0008-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-09-18 |
| Published | 2024-10-16 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | 123herbals |
| Distribution | n/a |
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
Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.
Identifiers
| code_info | All lots within expiry |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0008-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.