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Stop using now Drug recall · FDA · Published April 5, 2019

Kopi Jantan Coffee Recalled for Undeclared Erectile Drugs

FDA recalls Kopi Jantan coffee packages due to undeclared sildenafil and tadalafil. Check your lot and expiration date.

🇺🇸 FDA recall #D-1206-2019DrugKopi Jantan ›
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Recalling firmBrian P. Richardson3410 Delafield Ln · Dallas, TX 75227-5313
✎ GovInfoNow plain-language explainer

Brian P. Richardson is recalling Kopi Jantan Tradisional Natural Herbs Coffee because it contains undeclared drugs used for erectile dysfunction. The product was found to be tainted with sildenafil and tadalafil, which are FDA-approved prescription medications not allowed in this type of supplement. Because the safety and efficacy of these hidden ingredients have not been established, the product is subject to recall. Read more at govinfonow.com/recall/38956-kopi-jantan-coffee-recalled-for-undeclared-erectile-drugs.

Source Summary by GovInfoNow · govinfonow.com/recall/38956-kopi-jantan-coffee-recalled-for-undeclared-erectile-drugs · Updated October 11, 2026 · FDA enforcement record: FDA #D-1206-2019

Cite this page

“Kopi Jantan Coffee Recalled for Undeclared Erectile Drugs.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/38956-kopi-jantan-coffee-recalled-for-undeclared-erectile-drugs. Based on FDA recall #D-1206-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1206-2019%22&limit=1).

The FDA announced on April 5, 2019, that Brian P. Richardson voluntarily recalled Kopi Jantan Tradisional Natural Herbs Coffee because it was tainted with undeclared sildenafil and tadalafil. The agency classified the Class I recall as terminated.

How to tell if you have it

  • Brand: Kopi Jantan
  • Product: Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages
  • Manufacturer: Fikrysz (M) Sdn. Bhd., Kedah, Malaysia
  • UPC: 9 557205 060083
  • Lot code: All lots labeled with EXP 13 10 2020
  • Distribution: Nationwide in the USA
  • Units affected: 6000 packages

The hazard

According to the FDA, analysis found the product contained undeclared sildenafil and tadalafil, two drugs approved for treating male erectile dysfunction. This makes the coffee an unapproved drug for which safety and efficacy have not been established.

Context

GovInfoNow's records show Brian P. Richardson has one other recall on record since May 25, 2017. On May 25, 2017, the company recalled CaverFlo Natural Herbal Coffee for containing sildenafil and tadalafil. Other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (Dec. 15, 2025), Buy-Herbal Kian Pee Wan Capsules (March 21, 2026), and Shoolin Pharma Chem Sildenafil Recall (Aug. 3, 2026).

How to tell if you have this one

Look for Kopi Jantan Tradisional Natural Herbs Coffee in 13g individual packages manufactured by Fikrysz (M) Sdn. Bhd. in Kedah, Malaysia. Check the label for UPC 9 557205 060083 and an expiration date of 13 10 2020.

  • Brand
    Kopi Jantan
  • Product
    Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not drink or use the Kopi Jantan coffee packages due to the presence of undeclared prescription drugs.

  2. Discard or return the item

    Dispose of the product safely or return it to the place of purchase if possible, as no specific remedy is provided in this record.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.8 years after the firm started it.

1. Firm started the recall: Apr 5, 201912. FDA classified it Class I: Apr 22, 201923. Published in FDA’s Enforcement Report: Apr 24, 201934. FDA terminated the recall: Jan 19, 2022420192022
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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

✎ GovInfoNow

Questions people ask

Where was this product sold?

The recalled coffee was distributed nationwide in the USA.

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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 qwen3.6:35b-a3b on October 11, 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