Recall Radar

Disclaimer: Recall Radar is an informational summary of public FDA enforcement reports. It is not medical advice. Always confirm details with the FDA, the company, a pharmacist, or a doctor before making health decisions.

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Class IDrug

Kian Pee Wan Capsules recall

Summary

Buy-Herbal is recalling Kian Pee Wan Capsules (drug). According to the FDA report, the reason is: Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine. The FDA rated this a Class I: most serious: there is a reasonable chance the product could cause serious health problems or death. Recall status: Ongoing.

Understanding this recall

What happened

Buy-Herbal is recalling Kian Pee Wan capsules, sold to consumers through an eBay third-party seller, because they contain the undeclared drug ingredients dexamethasone (a steroid) and cyproheptadine (an antihistamine).

Why it matters

Products sold as supplements or herbal remedies sometimes contain hidden drug ingredients or unapproved stimulants. People taking them can't know what dose they're getting, the ingredients can interact with other medicines, and stimulants such as DMAA have been linked to raised blood pressure and heart problems. The FDA has repeatedly warned consumers about hidden ingredients in these kinds of products. Stopping hidden steroids suddenly after long-term use can also cause problems, so talk to a doctor before stopping.

Who should pay attention

Anyone who bought Kian Pee Wan capsules online.
Distribution in the FDA report: Product was sold to individual consumers via ebay third party seller.

How to check your product

The report says all lots within expiry are affected.
Codes listed by the FDA: All lots within expiry.

Based only on the FDA enforcement record plus general public-health background on this type of hazard. Not medical advice; if you have symptoms or concerns, contact a doctor or pharmacist.

Details from the FDA report

Product
Kian Pee Wan Capsules, 30-count bottles
Reason
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
Lot / code info
All lots within expiry.
Quantity
71 bottles
Distribution
Product was sold to individual consumers via ebay third party seller.
Recalling company
Buy-Herbal, Flushing, NY United States
Recall started
March 21, 2026
FDA report date
August 19, 2026
Classification
Class I: Most serious: there is a reasonable chance the product could cause serious health problems or death.
Voluntary / mandated
Voluntary: Firm initiated
Status
Ongoing
Recall number
D-0769-2026

What to do

View the FDA source record (openFDA) · FDA recalls page

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