Nhan Sam Tuyet Lien Truy Phong Hoan recall
FDA recall D-0177-2025 · initiated Dec 12, 2024
Buy-Herbal recalled Nhan Sam Tuyet Lien Truy Phong Hoan in Dec 2024 — an FDA Class I recall (D-0177-2025) because Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine.
Most serious — a reasonable probability that use will cause serious harm or death.
Why it was recalled
Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine
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: 26 bottles
Details
- Product
- Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles, Manufactured by Yee Hong Pharmaceuticals, SDN, Penang, Malasia.
- Recalling company
- Buy-Herbal
- Classification
- Class I
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- U.S Nationwide.
- Initiated
- Dec 12, 2024
- FDA report date
- Jan 15, 2025
Frequently asked
- Was Nhan Sam Tuyet Lien Truy Phong Hoan recalled?
- Buy-Herbal recalled Nhan Sam Tuyet Lien Truy Phong Hoan in Dec 2024 — an FDA Class I recall (D-0177-2025) because Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine. Most serious — a reasonable probability that use will cause serious harm or death.
- Why was Nhan Sam Tuyet Lien Truy Phong Hoan recalled?
- Per the FDA enforcement record, the reason for recall D-0177-2025 was: Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine
- Is a recalled Nhan Sam Tuyet Lien Truy Phong Hoan 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 Nhan Sam Tuyet Lien Truy Phong Hoan are affected?
- Distributed: U.S Nationwide.. The recall covers these lots — All codes, unknown expiration dates all before 05/2030.. 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-0177-2025.