123Herbals Vail-Bon Jie Yang Wan capsules Recall: FDA Class I

Why it was recalled

Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.

Product description

Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn. Bhd., No 1, Lorong Mengkudu, Taman Mengkudu, 14100 Juru, Malaysia.

Lot numbers, UPCs & expiration codes

All lots within expiry

Where it was sold

Distributed via Amazon and 123Herbals.com website

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-0008-2025
Classification: Class I
Status: Ongoing
Recall initiated: Sep 18, 2024
FDA report date: Oct 16, 2024
Quantity: unknown
Recall type: Voluntary: Firm initiated
Recalling firm: 123Herbals

Original FDA data

Every field from FDA enforcement report D-0008-2025, exactly as published.

Show all FDA fields

City: Rosemead
State: CA
Status: Ongoing
Country: United States
Event ID: 95391
Address: 7214 Berne St
Code information: All lots within expiry
Postal code: 91770-3844
Report date: Oct 16, 2024
Product type: Drugs
Recall number: D-0008-2025
Classification: Class I
Recalling firm: 123Herbals
Product quantity: unknown
Reason for recall: Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn. Bhd., No 1, Lorong Mengkudu, Taman Mengkudu, 14100 Juru, Malaysia.
Distribution pattern: Distributed via Amazon and 123Herbals.com website
Recall initiation date: Sep 18, 2024
Initial firm notification: E-Mail
Center classification date: Oct 10, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0008-2025, published Oct 16, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

123Herbals Vail-Bon Jie Yang Wan capsules Recall

Summary