CLASS I ONGOING Drug recall · Reported 15 Jan 2025 · FDA Enforcement Report
Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules recalled by Buy-Herbal
Buy-Herbal is recalling Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, distributed nationwide in the US. The recall was initiated on 12 Dec 2024 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0177-2025
- FDA event ID
- 95980
- Recalling firm
- Buy-Herbal, Flushing, NY
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 12 Dec 2024
- FDA classified
- 3 Jan 2025
- Reported
- 15 Jan 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
Timeline
| 12 Dec 2024 | Recall initiated by company | |
| 3 Jan 2025 | Classified by FDA | +22 days |
| 15 Jan 2025 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine
Product as listed by the FDA
Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles, Manufactured by Yee Hong Pharmaceuticals, SDN, Penang, Malasia.
Where it was distributed
U.S Nationwide.
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine
Which lots are affected?
All codes, unknown expiration dates all before 05/2030.
Where was it sold?
U.S Nationwide.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Buy-Herbal
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Kian Pee Wan Capsules recalled by Buy-Herbal | Buy-Herbal | Labeling Errors | NY |