Kian Pee Wan Capsules Recall
Kian Pee Wan Capsules, 30-count bottles
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was Kian Pee Wan Capsules recalled?
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.
Full product description
Kian Pee Wan Capsules, 30-count bottles
Which lot codes, UPCs or models are affected?
All lots within expiry.
- Agency record number
- D-0769-2026
- Product
- Kian Pee Wan Capsules, 30-count bottles
- Recalling firm
- Buy-Herbal
- Quantity
- 71 bottles
- Distribution
- Product was sold to individual consumers via ebay third party seller.
- Recall started
- March 21, 2026
- Report date
- August 19, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)