Drug recall
Kian Pee Wan Capsules, 30-count bottles
FDA recall event 98650 · Class I · Buy-Herbal
Key facts
| Event ID | 98650 |
|---|---|
| Recall numbers | D-0769-2026 |
| Recalling firm | Buy-Herbal |
| Product type | Drugs |
| Products | Kian Pee Wan Capsules, 30-count bottles |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine. |
| Initiation date | Mar 21, 2026 |
| Report date | Aug 19, 2026 |
| City | Flushing |
| State | NY |
| Country | United States |
| FEI number | 3031853195 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: