Kian Pee Wan Capsules recall
FDA recall D-0769-2026 · initiated Mar 21, 2026
Buy-Herbal recalled Kian Pee Wan Capsules in Mar 2026 — an FDA Class I recall (D-0769-2026) because Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
Most serious — a reasonable probability that use will cause serious harm or death.
Why it was recalled
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
Sold unapproved, or found to contain something undeclared
The product should not have been on sale in this form — often a supplement found to contain a hidden prescription drug.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 71 bottles
Details
- Product
- Kian Pee Wan Capsules, 30-count bottles
- Recalling company
- Buy-Herbal
- Classification
- Class I
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- Product was sold to individual consumers via ebay third party seller.
- Initiated
- Mar 21, 2026
- FDA report date
- Aug 19, 2026
Frequently asked
- Was Kian Pee Wan Capsules recalled?
- Buy-Herbal recalled Kian Pee Wan Capsules in Mar 2026 — an FDA Class I recall (D-0769-2026) because Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine. Most serious — a reasonable probability that use will cause serious harm or death.
- Why was Kian Pee Wan Capsules recalled?
- Per the FDA enforcement record, the reason for recall D-0769-2026 was: Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
- Is a recalled Kian Pee Wan Capsules dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of Kian Pee Wan Capsules are affected?
- Distributed: Product was sold to individual consumers via ebay third party seller.. The recall covers these lots — All lots within expiry.. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0769-2026.