Vail-Bon: Vail-Bon Jie Yang Wan — FDA announcement Sep 20, 2024

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Sep 20, 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
Reason
Product is tainted with dexamethasone and chlorpheniramine
Classification
Not supplied
Recalling firm
123herbals
Quantity
Not supplied
Agency-reported status
Company recall announcement
Source record identifier
19569f7b7348db08

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Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityThe product is used to treat skin disease, eczema, itch and is packaged in 30-count plastic bottles. The affected Vail-Bon Jie Yang Wan capsules include all lot numbers and expirations. Vail- Bon Jie Yang Wan capsules were distributed nationwide on 123herbals.com and online retailers including Amazon.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

The product is used to treat skin disease, eczema, itch and is packaged in 30-count plastic bottles. The affected Vail-Bon Jie Yang Wan capsules include all lot numbers and expirations. Vail- Bon Jie Yang Wan capsules were distributed nationwide on 123herbals.com and online retailers including Amazon.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Fda listing date
Sep 20, 2024
Company announcement date
Sep 18, 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.

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