Kian Pee Wan Capsules, 30-count bottles was recalled on March 21, 2026 in cooperation with the U.S. Food and Drug Administration because marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine..
Kian Pee Wan Capsules, 30-count bottles
All lots within expiry.
Units affected: 71 bottles
Where it was sold: Product was sold to individual consumers via ebay third party seller.
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
Class I is the most serious FDA recall level: using or being exposed to the product could cause serious health problems or death.
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: Buy-Herbal
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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The glued knot on the elastic cord can become untied on the recalled product, allowing young children access to the small wooden and plastic pieces, posing a risk of serious injury or death from choking and ingestion hazards.
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