Kian Pee Wan Capsules, 30-count bottles

FDA recall notice · announced August 19, 2026 · Buy-herbal

Class I FDA/FSIS Class I: reasonable probability that use will cause serious adverse health consequences or death.

The product

Kian Pee Wan Capsules, 30-count bottles

Reason for recall

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

Notes

Distribution: Product was sold to individual consumers via ebay third party seller.
Lot/code information: All lots within expiry.
Quantity: 71 bottles
Status: Ongoing
Products in this recall event:
- Kian Pee Wan Capsules, 30-count bottles (D-0769-2026)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.