Skip to content
Stop using now Drug recall · FDA · Published December 12, 2024

Buy-Herbal Recalls Herbal Capsules for Undeclared Drugs

Buy-Herbal recalls 26 bottles of Nhan Sam capsules due to undeclared Furosemide, Dexamethasone, and Chlorpheniramine. Check your bottle.

🇺🇸 FDA recall #D-0177-2025DrugBuy-Herbal ›
Take action

Contact the company

Recalling firmBuy-Herbal13661 41st Ave, Box 239 · Flushing, NY 11355-2464
✎ GovInfoNow plain-language explainer

Buy-Herbal is recalling 26 bottles of Nhan Sam Tuyet Lien Truy Phong Hoan capsules because they contain undeclared prescription drugs: Furosemide, Dexamethasone, and Chlorpheniramine. The product was manufactured by Yee Hong Pharmaceuticals in Penang, Malaysia. This recall is classified as Class I, indicating a serious health risk. Read more at govinfonow.com/recall/32366-buy-herbal-recalls-herbal-capsules-for-undeclared-drugs.

Source Summary by GovInfoNow · govinfonow.com/recall/32366-buy-herbal-recalls-herbal-capsules-for-undeclared-drugs · Updated October 9, 2026 · FDA enforcement record: FDA #D-0177-2025

Cite this page

“Buy-Herbal Recalls Herbal Capsules for Undeclared Drugs.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/32366-buy-herbal-recalls-herbal-capsules-for-undeclared-drugs. Based on FDA recall #D-0177-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0177-2025%22&limit=1).

The FDA announced on Dec. 12, 2024, that Buy-Herbal is voluntarily recalling Nhan Sam Tuyet Lien Truy Phong Hoan Capsules because they are tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine. The agency classified the Class I recall as ongoing.

How to tell if you have it

  • Brand: Buy-Herbal
  • Product: Nhan Sam Tuyet Lien Truy Phong Hoan Capsules
  • Quantity: 30-Count Bottles
  • Manufacturer: Yee Hong Pharmaceuticals, SDN, Penang, Malasia
  • Expiration dates: All codes, unknown expiration dates all before 05/2030
  • Units affected: 26 bottles

The hazard

FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine. The products were marketed without an Approved NDA/ANDA.

Context

GovInfoNow's records show Buy-Herbal has 1 other recall on record since 2026-03-21. On 2026-03-21, Buy-Herbal Kian Pee Wan Capsules were recalled for undeclared drug ingredients dexamethasone and cyproheptadine. Other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15), SILINTAN 25-pill bottle (2025-10-20) and Asclemed Duloxetine Capsules (2026-05-14).

How to tell if you have this one

Look for 30-count bottles of Nhan Sam Tuyet Lien Truy Phong Hoan Capsules manufactured by Yee Hong Pharmaceuticals in Penang, Malaysia. The record states all codes have unknown expiration dates before May 2030. Distribution was nationwide in the U.S.

  • Brand
    Buy-Herbal
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume the capsules as they contain undeclared prescription drugs.

  2. Discard or return the item

    The recall record does not specify a return address or refund process, so dispose of the product safely.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “U.S Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 34 days after the firm started it.

1. Firm started the recall: Dec 12, 202412. FDA classified it Class I: Jan 3, 202523. Published in FDA’s Enforcement Report: Jan 15, 2025320242025
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest drug recalls

Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0177-2025 (December 12, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0177-2025 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA