Brian P. Richardson recalls Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah,
FDA recalls Kopi Jantan Tradisional Natural Herbs Coffee due to undeclared sildenafil and tadalafil, unapproved drugs with unknown safety.
Stop using this now
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with undeclared sildenafil and tadalafil, two FDA approved drugs for the treatment of male erectile dysfunction, making this an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Contact the company & request your remedy
What happened, in plain English
Brian P. Richardson is recalling Kopi Jantan Tradisional Natural Herbs Coffee packages because they contain undeclared sildenafil and tadalafil, two drugs approved for erectile dysfunction but not approved for use in coffee. This makes the product unsafe as its safety and effectiveness have not been established by the FDA. Read more at govinfonow.com/recall/38956-kopi-jantan-coffee-recall-unapproved-drugs-found-in-product.
Source Summary by GovInfoNow · govinfonow.com/recall/38956-kopi-jantan-coffee-recall-unapproved-drugs-found-in-product · Updated October 5, 2026 · FDA enforcement record: FDA #D-1206-2019
Cite this page
“Kopi Jantan Coffee Recall: Unapproved Drugs Found in Product.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38956-kopi-jantan-coffee-recall-unapproved-drugs-found-in-product. Based on FDA recall #D-1206-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1206-2019%22&limit=1).
Why it’s dangerous
The coffee contains undeclared sildenafil and tadalafil, which are FDA-approved drugs for erectile dysfunction. These drugs were found in the product through FDA analysis, meaning the coffee is unapproved and lacks established safety and effectiveness data.
Who’s affected
Anyone who owns or uses Kopi Jantan Tradisional Natural Herbs Coffee packages labeled with expiration date 10/13/2020. People most at risk are those who consume the coffee without knowing it contains unapproved drugs.
How to tell if you have this one
Check for Kopi Jantan Tradisional Natural Herbs Coffee packages with 13g individual servings, manufactured by Fikrysz (M) Sdn. Bhd. in Kedah, Malaysia, and expiration date 10/13/2020.
- Brand
Brian P. Richardson- Product
Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah- Category
Drug
What to do — step by step
Stop Using Now
Immediately stop using Kopi Jantan Tradisional Natural Herbs Coffee packages as they contain unapproved drugs with unknown safety.
Questions people ask
Why is this coffee being recalled?
FDA analysis found undeclared sildenafil and tadalafil, two drugs approved for erectile dysfunction, making this an unapproved product with unknown safety.
What should I do if I have this coffee?
Stop using it immediately as it contains unapproved drugs with unknown safety.
Is this coffee safe to drink?
No, the coffee contains unapproved drugs that have not been tested for safety and effectiveness.
Contact Brian P. Richardson
We’ve drafted a message you can send Brian P. Richardson to request your refund or repair — edit it as you like.
Subject: Recall D-1206-2019 — Brian P. Richardson Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufact Hello, I own a Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah that is covered by recall D-1206-2019 from Brian P. Richardson. 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.
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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-1206-2019 (April 5, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1206-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.
