Vail-Bon Jie Yang Wan capsules recall
FDA recall D-0008-2025 · initiated Sep 18, 2024
123Herbals recalled Vail-Bon Jie Yang Wan capsules in Sep 2024 — an FDA Class I recall (D-0008-2025) because Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.
Most serious — a reasonable probability that use will cause serious harm or death.
Why it was recalled
Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.
Sold unapproved, or found to contain something undeclared
The product should not have been on sale in this form — often a supplement found to contain a hidden prescription drug.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: unknown
Details
- 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.
- Recalling company
- 123Herbals
- Classification
- Class I
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- Distributed via Amazon and 123Herbals.com website
- Initiated
- Sep 18, 2024
- FDA report date
- Oct 16, 2024
Frequently asked
- Was Vail-Bon Jie Yang Wan capsules recalled?
- 123Herbals recalled Vail-Bon Jie Yang Wan capsules in Sep 2024 — an FDA Class I recall (D-0008-2025) because Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine. Most serious — a reasonable probability that use will cause serious harm or death.
- Why was Vail-Bon Jie Yang Wan capsules recalled?
- Per the FDA enforcement record, the reason for recall D-0008-2025 was: Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.
- Is a recalled Vail-Bon Jie Yang Wan capsules dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of Vail-Bon Jie Yang Wan capsules are affected?
- Distributed: Distributed via Amazon and 123Herbals.com website. The recall covers these lots — All lots within expiry. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0008-2025.