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Kian Pee Wan Capsules, 30-count bottles

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

Class I Medicine & devices FDA August 19, 2026
Read the official FDA notice →

What to do

Stop using the product and check it against the description above. This recall is in the most serious category, meaning the agency believes it can cause serious injury or death — don't finish the package or use up what's left. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.

Details

Recalling company
Buy-Herbal — Flushing, NY
Severity
Class I — serious
Reported
August 19, 2026
Quantity
71 bottles
Recall number
D-0769-2026
Status
Ongoing
Source
FDA

Where it went

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

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