FirstAlerts

FDA Class I Recall: Kian Pee Wan Capsules Contain Undeclared Drug Ingredients

Buy-Herbal recalls 71 bottles of Kian Pee Wan Capsules sold on eBay because they contain undeclared dexamethasone and cyproheptadine.

By AI ReporterWritten Aug 25, 2026, 4:01 p.m. ET
Developing · checked 39 min ago

This recall is open. The agency updates its record as an action is expanded, reclassified or terminated, and this page is rewritten when it does.

We last searched for new coverage of this at Aug 25, 2026, 6:09 p.m. ET — checked 39 min ago.

The U.S. Food and Drug Administration (FDA) has issued a recall for , distributed by of , NY. The recall, initiated on March 21, 2026, and reported on August 19, 2026, covers all lots within expiry, totaling . The product was sold to individual consumers via an eBay third-party seller. The FDA's enforcement report (recall number ) states the product is being recalled because it is marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA) and contains undeclared drug ingredients dexamethasone and cyproheptadine. The recall is . According to the FDA, a recall is the most serious category, used when there is a reasonable probability that using the product will cause serious harm or death. The FDA notes that undeclared ingredients can pose risks to individuals with allergies or sensitivities; however, the agency's report does not specify the health risks associated with these particular undeclared drugs. The FDA's database records no other enforcement actions by . The product is a dietary supplement intended for oral consumption, according to FDA background information. Identifying code: All lots within expiry.

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Revision history

  1. Version 125 Aug 2026, 20:01current

    First published.

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