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Drug recall · FDA · Published October 22, 2019

Green Lumber Holdings, LLC recalls Green Lumber Natural Fuel For Men capsule, packaged in packs of 2, 4 and 10 capsules, 2618 San Miguel Drive, Suite

FDA recalls Green Lumber Natural Fuel For Men capsules due to undeclared tadalafil, an erectile dysfunction drug. Products sold in packs of 2, 4, or 10 capsules with specific lot numbers are affected. Consumers should stop using and contact the manufacturer for details.

🇺🇸 FDA recall #D-0351-2020DrugGreen Lumber ›
Take action

Contact the company & request your remedy

Recalling firmGreen Lumber Holdings, LLC2855 E Coast Hwy Ste 228, N/A · Corona Del Mar, CA 92625-2200
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

The FDA has recalled Green Lumber Natural Fuel For Men capsules because they contain undeclared tadalafil, a drug approved for erectile dysfunction. This poses a risk of unintended medication effects since the product was marketed without proper FDA approval. Consumers should stop using the product immediately and contact the manufacturer for further instructions. Read more at govinfonow.com/recall/37801-green-lumber-natural-fuel-for-men-capsules-contain-undeclared-tadalafil.

Source Summary by GovInfoNow · govinfonow.com/recall/37801-green-lumber-natural-fuel-for-men-capsules-contain-undeclared-tadalafil · Updated October 5, 2026 · FDA enforcement record: FDA #D-0351-2020

Cite this page

“Green Lumber Natural Fuel For Men Capsules Contain Undeclared Tadalafil - FDA Recall.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37801-green-lumber-natural-fuel-for-men-capsules-contain-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).

Why it’s dangerous

The capsules contain tadalafil, a drug approved for erectile dysfunction, but were marketed without FDA approval. This means the product could cause unintended side effects or interactions with other medications without proper oversight.

Who’s affected

Anyone who purchased Green Lumber Natural Fuel For Men capsules with lot numbers XC12 through XC06 (expiring 12/2020 to 06/2022) is affected. Men who use these products for health reasons may be at higher risk due to the presence of an undeclared prescription drug.

How to tell if you have this one

Check the product label for lot numbers XC12 (expiring 12/2020), XC06 (expiring 06/2022), or XC10 (expiring 10/2021). Products sold in packs of 2, 4, or 10 capsules from Green Lumber Holdings, LLC in Newport Beach, CA are affected.

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

What to do — step by step

  1. Stop Using Now

    Immediately stop using the recalled Green Lumber Natural Fuel For Men capsules as they contain undeclared tadalafil.

✎ GovInfoNow

Questions people ask

Why was this product recalled?

The FDA found that the product contains undeclared tadalafil, an FDA-approved drug for erectile dysfunction, but was marketed without proper approval.

What lot numbers are affected?

Lot numbers XC12 (expiring 12/2020), XC06 (expiring 06/2022), XC10 (expiring 10/2021), XC02 (expiring 02/2022), and XC04 (expiring 04/2022) are affected.

How can I contact the manufacturer?

The manufacturer, Green Lumber Holdings, LLC, can be reached at (949) 426-8622.

Take action

Contact Green Lumber

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

Subject: Recall D-0351-2020 — Green Lumber Green Lumber

Hello,

I own a Green Lumber that is covered by recall D-0351-2020 from Green Lumber.

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-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 qwen3:4b 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.
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