Class IOngoing

Nhan Sam Tuyet Lien Truy Phong Hoan recall

FDA recall D-0177-2025 · initiated Dec 12, 2024

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

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

What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Source: openFDA Drug Enforcement record D-0177-2025 ↗

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