FDAFDA · Food and drugs·Recall number D-0769-2026
Kian Pee Wan Capsules, 30-count bottles
Published August 19, 2026 · Recall initiated: March 21, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Buy-Herbal
- Distributor
- Product was sold to individual consumers via ebay third party seller.
- Lot
- All lots within expiry.
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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