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CLASS I · SeriousFDA

Buy-Herbal recalls Kian Pee Wan Capsules

📅 Mar 21, 2026 · 📍 See notice
Recalling company
Buy-Herbal
Product
Kian Pee Wan Capsules, 30-count bottles
Reason
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
Classification
Class I – a reasonable probability that use will cause serious adverse health consequences or death
Recall date
Mar 21, 2026
Reported
Aug 19, 2026
Distribution
Product was sold to individual consumers via ebay third party seller.
Status
Ongoing
Quantity
71 bottles
Lot / codes
All lots within expiry.
Company location
Flushing, NY
Recall type
Voluntary: Firm initiated
Recall number
D-0769-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number D-0769-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.