← FDA ENFORCEMENT
D-0177-2025Class I

Buy-Herbal

Recalling firm
Buy-Herbal
Product type
Drug
Status
Ongoing
Report date
2025-01-15
Distribution
U.S Nationwide.
Firm state
NY
Product quantity
26 bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine

Product description

Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles, Manufactured by Yee Hong Pharmaceuticals, SDN, Penang, Malasia.

Code / lot info

All codes, unknown expiration dates all before 05/2030.

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.