FDA Drugs recall ·
Vail-Bon Jie Yang Wan capsules, 30-count bottle… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0008-2025
- Date
- (initiated September 18, 2024)
- Company / brand
- 123Herbals
7214 Berne St, Rosemead, CA, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- unknown
- Hazard tags
- Undeclared allergen
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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.
Why was it recalled?
Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All lots within expiry
Distribution
Distributed via Amazon and 123Herbals.com website
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0008-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.