FDAClass I · Drug · Recall D-0769-2026 · Recalled August 19, 2026

Kian Pee Wan Capsules recall — Buy-Herbal

Agency report date: August 19, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Kian Pee Wan Capsules
Company / brand: Buy-Herbal
Lot / serial / date codes: All lots within expiry.
Distribution: Product was sold to individual consumers via ebay third party seller.

Agency product description and boundaries

Kian Pee Wan Capsules, 30-count bottles

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Kian Pee Wan Capsules

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: D-0769-2026
Brand: Buy-Herbal
Classification: Class I
Units affected: 71 bottles
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Kian Pee Wan Capsules

Companies & origin

Recalling firm location: Flushing, NY, United States
Firm address: 13661 41st Ave, Box 239, 11355-2464

Identifying details (verbatim from the notice)

Product codes / lots: All lots within expiry.
Distribution: Product was sold to individual consumers via ebay third party seller.
Firm notified the public via: E-Mail
FDA event ID: 98650
Recall initiated: March 21, 2026
FDA classified: August 17, 2026
FDA report date: August 19, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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