US Drug Recall Register
Class I · High risk Ongoing Initiated Mar 21, 2026 (6 months ago)

Kian Pee Wan Capsules, 30-count bottles

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.

What was recalled

Kian Pee Wan Capsules, 30-count bottles

Recalling firm
Buy-Herbal
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0769-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.