Recall archive / FDA drug enforcement
Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn. Bhd., No 1, Lorong Mengkudu, Taman Me... — FDA record D-0008-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Sep 18, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class I
- Recalling firm
- 123Herbals
- Quantity
- unknown
- Agency-reported status
- Ongoing
- Source record identifier
- D-0008-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | All lots within expiry |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Distributed via Amazon and 123Herbals.com website
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Oct 16, 2024
- Recall initiation date
- Sep 18, 2024
- Center classification date
- Oct 10, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.