Kian Pee Wan Capsules, 30-count bottles
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
| Recalling firm | Buy-Herbal |
|---|---|
| Reason | Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine. |
| Risk class | Class I (Class I · high risk) |
| Status | Ongoing |
| Report date | Aug 19, 2026 |
| Initiated | Mar 21, 2026 |
| Region | NY, United States |
| Distribution | Product was sold to individual consumers via ebay third party seller. |
| Quantity | 71 bottles |
| Code/Lot | All lots within expiry. |
| Type | Voluntary: Firm initiated |
| Recall number | D-0769-2026 |
Official source
U.S. FDA — Recalls, Market Withdrawals & Safety Alerts fda.gov ↗You can re-verify each item on the official FDA site using its recall number. (Recall number: D-0769-2026)
openFDA (U.S. Food & Drug Administration) — food/drug/device enforcement · CC0 1.0 (public domain)
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