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Stop using now Drug recall · FDA · Published October 22, 2019

Green Lumber Natural Fuel For Men Recall: Undeclared Tadalafil

Green Lumber Holdings recalls Natural Fuel For Men capsules due to undeclared Tadalafil. Check lot numbers XC12, XC06, XC10, XC02, XC04 for expiration dates through 2022.

🇺🇸 FDA recall #D-0351-2020DrugGreen Lumber ›
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Recalling firmGreen Lumber Holdings, LLC2855 E Coast Hwy Ste 228 · Corona Del Mar, CA 92625-2200
✎ GovInfoNow plain-language explainer

Green Lumber Holdings, LLC is recalling its Green Lumber Natural Fuel For Men capsule because it contains undeclared Tadalafil, a prescription drug for erectile dysfunction. The product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). Approximately 30,000 capsules were distributed to the United States and Canada via email. Read more at govinfonow.com/recall/37801-green-lumber-natural-fuel-for-men-recall-undeclared-tadalafil.

Source Summary by GovInfoNow · govinfonow.com/recall/37801-green-lumber-natural-fuel-for-men-recall-undeclared-tadalafil · Updated October 11, 2026 · FDA enforcement record: FDA #D-0351-2020

Cite this page

“Green Lumber Natural Fuel For Men Recall: Undeclared Tadalafil.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/37801-green-lumber-natural-fuel-for-men-recall-undeclared-tadalafil. Based on FDA recall #D-0351-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0351-2020%22&limit=1).

The Food and Drug Administration announced on Oct. 22, 2019, that Green Lumber Holdings, LLC voluntarily recalled its Natural Fuel For Men Capsule because the product was marketed without an approved New Drug Application and contained undeclared Tadalafil. The FDA said the recall affects approximately 30,000 capsules distributed in the United States and Canada.

How to tell if you have it

  • Brand: Green Lumber
  • Product: Natural Fuel For Men Capsule
  • Lot codes: XC12 (EXP 12/2020), XC06 (EXP06/2021), XC10 (EXP 10/2021), XC02 (EXP 02/2022), XC04 (EXP 04/2022), XC06 (EXP06/2022)
  • Pack sizes: 2, 4, and 10 capsules
  • Distribution: United States and Canada

The hazard

The FDA said the product contains undeclared Tadalafil, an FDA-approved drug for the treatment of erectile dysfunction. The agency classified the recall as Class I, indicating a reasonable probability that the use of the product will cause serious adverse health consequences or death.

Context

GovInfoNow's records show Green Lumber Holdings, LLC has one other recall on record since 2025-08-28 involving Natural Fuel For Men Capsules for an FDA-approved drug risk. Other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15), Buy-Herbal Kian Pee Wan Capsules Recall (2026-03-21), and Shoolin Pharma Chem Tadalafil Recall (2026-08-03).

How to tell if you have this one

Look for Green Lumber Natural Fuel For Men capsules packaged in packs of 2, 4, or 10. Check the lot numbers and expiration dates: Lot XC12 (EXP 12/2020), Lot XC06 (EXP 06/2021), Lot XC10 (EXP 10/2021), Lot XC02 (EXP 02/2022), and Lot XC04 (EXP 04/2022). The product was distributed in the United States and Canada.

  • Brand
    Green Lumber
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume any Green Lumber Natural Fuel For Men capsules if you have them, as they contain undeclared Tadalafil.

  2. Check your lot numbers

    Verify if your product matches the recalled lots: XC12, XC06, XC10, XC02, or XC04 with expiration dates through 2022.

  3. Contact the manufacturer

    Reach out to Green Lumber Holdings, LLC at (949) 426-8622 for further instructions on disposal or return.

How this recall unfolded

Recall timeline

FDA terminated this recall 3.4 years after the firm started it.

1. Firm started the recall: Oct 22, 201912. Published in FDA’s Enforcement Report: Nov 13, 201923. FDA classified it Class I: Nov 15, 201934. FDA terminated the recall: Mar 22, 2023420192023
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  4. FDA terminated the recall

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

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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-0351-2020 (October 22, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0351-2020 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