FDA Drugs recall ·
Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0177-2025
- Date
- (initiated December 12, 2024)
- Company / brand
- Buy-Herbal
13661 41st Ave, Flushing, NY, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 26 bottles
- Hazard tags
- Undeclared allergen
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles, Manufactured by Yee Hong Pharmaceuticals, SDN, Penang, Malasia.
Why was it recalled?
Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All codes, unknown expiration dates all before 05/2030.
Distribution
U.S Nationwide.
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0177-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.