Skip to content
Drug recall · FDA · Published July 17, 2017

BESTHERBS COFFEE LLC recalls New Kopi Jantan Tradisional Natural Herbs Coffee, packaged in 13 gram red packets, and each box contains 25 packets,

Bestherbs Coffee LLC recalls 25-packet boxes of New Kopi Jantan Tradisional Natural Herbs Coffee due to undeclared desmethyl carbodenafil and milk. Consumers should stop using the product immediately.

🇺🇸 FDA recall #D-1144-2017DrugBestherbs Coffee ›
Take action

Contact the company & request your remedy

Emailbestherbscoffee@yahoo.com
Recalling firmBESTHERBS COFFEE LLC2420 E Arkansas Ln Ste 216, N/A · Arlington, TX 76014-1753
Opens pre-filled in Gmail, Outlook, Yahoo, or your mail app.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Bestherbs Coffee LLC is recalling 25-packet boxes of New Kopi Jantan Tradisional Natural Herbs Coffee because it contains undeclared desmethyl carbodenafil and milk. This could pose health risks as the product was marketed without proper FDA approval. Read more at govinfonow.com/recall/41442-bestherbs-coffee-recall-undeclared-ingredients-in-new-kopi-jantan-coffee.

Source Summary by GovInfoNow · govinfonow.com/recall/41442-bestherbs-coffee-recall-undeclared-ingredients-in-new-kopi-jantan-coffee · Updated October 7, 2026 · FDA enforcement record: FDA #D-1144-2017

Cite this page

“Bestherbs Coffee Recall: Undeclared Ingredients in New Kopi Jantan Coffee.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41442-bestherbs-coffee-recall-undeclared-ingredients-in-new-kopi-jantan-coffee. Based on FDA recall #D-1144-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1144-2017%22&limit=1).

Why it’s dangerous

The coffee was marketed without an approved FDA registration, containing undeclared desmethyl carbodenafil (a drug) and milk. This could cause health issues for consumers, especially those with allergies or sensitivities to these ingredients.

Who’s affected

Anyone who owns or uses the New Kopi Jantan Tradisional Natural Herbs Coffee in 13-gram red packets, sold in boxes of 25. People with allergies to milk or desmethyl carbodenafil are at higher risk.

How to tell if you have this one

Check for 13-gram red packets in boxes of 25, made in Malaysia with a UPC code 557205060083. The product was distributed by Bestherbs Coffee LLC in the US and expired May 24, 2018.

  • Brand
    Bestherbs Coffee
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using the recalled coffee product as it contains undeclared ingredients that could cause health risks.

✎ GovInfoNow

Questions people ask

Is this coffee safe to drink?

No, the coffee contains undeclared desmethyl carbodenafil and milk, which were not approved by the FDA, so it is not safe to consume.

How can I check if my coffee is recalled?

Look for 13-gram red packets in boxes of 25 with UPC 557205060083, made in Malaysia and expiring May 24, 2018.

What should I do if I have the recalled coffee?

Stop using it immediately and contact Bestherbs Coffee LLC at bestherbscoffee@yahoo.com for further instructions.

Take action

Contact Bestherbs Coffee

We’ve drafted a message you can send Bestherbs Coffee to request your refund or repair — edit it as you like.

Subject: Recall D-1144-2017 — Bestherbs Coffee Bestherbs Coffee

Hello,

I own a Bestherbs Coffee that is covered by recall D-1144-2017 from Bestherbs Coffee.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

Keep exploring

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Comments are reviewed before they appear. No links, ads, or personal attacks — those get removed.

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-1144-2017 (July 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1144-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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