FDA · Class I · August 19, 2026

Buy-Herbal recall: Kian Pee Wan Capsules

Buy-Herbal is recalling Kian Pee Wan Capsules – 71 bottles. The U.S. Food and Drug Administration published the recall on August 19, 2026; it began on March 21, 2026. Distributed Product was sold to individual consumers via ebay third party seller..

Most serious Class I is the most serious level: a reasonable probability that using or eating the product will cause serious health problems or death.

A pharmacy dispensing machine
Illustration: A pharmacy dispensing machine – not the recalled product. Photo: U.S. Air Force / Airman Trevor Calvert, public domain.
ProductKian Pee Wan Capsules
BrandBuy-Herbal
TypeDrugs
ClassificationClass I
Recall dateMarch 21, 2026
Published by FDAAugust 19, 2026
Quantity71 bottles
Recall ID98650
As listed by FDA

Recalled products

  1. Kian Pee Wan Capsules, 30-count bottles
    FDA recall number
    D-0769-2026
    Codes, lots and dates
    All lots within expiry.
    Quantity
    71 bottles
    Classification
    Class I
Exactly as the agency lists them

Identifiers and details

FDA event ID
98650
Initiated
Voluntary: Firm initiated
Status
Ongoing
Firm location
Flushing, NY, United States

Why it was recalled

The reason the FDA lists: “Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.”

Where it was sold

Distribution as the FDA records it: “Product was sold to individual consumers via ebay third party seller.”

What to do

Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.

Official notice: FDA Enforcement Report record (event 98650, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.

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FAQ

About this recall

Is Buy-Herbal Kian Pee Wan Capsules recalled?

Yes. Buy-Herbal recalled it on March 21, 2026; FDA published it August 19, 2026 (Class I). Only the lots, dates or models listed on this page are included.

Why was it recalled?

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

What should I do if I have it?

Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.

Where was it sold?

Product was sold to individual consumers via ebay third party seller..

Recalls

More recalls

Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.

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