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Class IOngoing

Buy-Herbal recalls Kian Pee Wan Capsules

Recall date · record updated Aug 19, 2026 · Source: U.S. Food and Drug Administration (openFDA drug enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Buy-Herbal
Reason
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
Hazard
FDA Class I: a reasonable probability that use or exposure will cause serious adverse health consequences or death (FDA definition).
Who’s affected
Product was sold to individual consumers via ebay third party seller.
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=98650…

Products

  1. Kian Pee Wan Capsules, 30-count bottles

    Codes/lots: All lots within expiry.Quantity: 71 bottlesRecall no. D-0769-2026Class I

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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