Skip to content
Unrated Drug recall · FDA · Published August 28, 2025

Green Lumber Natural Fuel For Men Capsules: FDA-Approved Drug Risk

FDA found Green Lumber Natural Fuel For Men capsules contain tadalafil without proper approval. Consumers should check if they own these products and contact the manufacturer for details.

🇺🇸 FDA recall #D-0304-2026DrugGreen Lumber ›
Take action

Contact the company

Recalling firmGreen Lumber Holdings, LLC2855 E Coast Hwy Ste 228 · Corona Del Mar, CA 92625-2200
✎ GovInfoNow plain-language explainer

Green Lumber Holdings is recalling Natural Fuel For Men capsules because they contain tadalafil without FDA approval. This means the product is not legally approved and could pose health risks. Read more at govinfonow.com/recall/31821-green-lumber-natural-fuel-for-men-capsules-fda-approved-drug.

Source Summary by GovInfoNow · govinfonow.com/recall/31821-green-lumber-natural-fuel-for-men-capsules-fda-approved-drug · Updated August 17, 2026 · FDA enforcement record: FDA #D-0304-2026

Cite this page

“Green Lumber Natural Fuel For Men Capsules: FDA-Approved Drug Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31821-green-lumber-natural-fuel-for-men-capsules-fda-approved-drug. Based on FDA recall #D-0304-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0304-2026%22&limit=1).

The Food and Drug Administration announced on Aug. 28, 2025, that Green Lumber Holdings, LLC is recalling its Green Lumber Natural Fuel For Men capsules because they contain undeclared tadalafil. The agency said the product was marketed without an approved New Drug Application or Abbreviated New Drug Application.

How to tell if you have it

  • Brand: Green Lumber
  • Product: Green Lumber Natural Fuel For Men capsule
  • Packaging: 2, 4, 10, and 30-count blister packs
  • Lot code: LOT308EXP03/28

The hazard

The FDA said its analysis found the product to contain tadalafil. The agency classified the recall as Class I.

Context

GovInfoNow's records show Green Lumber Holdings, LLC has one other recall on record since Oct. 22, 2019, for the same product due to undeclared tadalafil. Other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (Dec. 15, 2025) and Shoolin Pharma Chem Tadalafil Recall (Aug. 3, 2026).

How to tell if you have this one

Check for capsules labeled 'Natural Fuel For Men' in blister packs of 2, 4, 10, or 30 counts. Products sold through GreenLumber.com with lot number LOT308EXP03/28 are affected.

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

What to do — step by step

  1. Check Product Details

    Look for capsules labeled 'Natural Fuel For Men' in blister packs of 2, 4, 10, or 30 counts.

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

Distributed nationwide.

Recall timeline

FDA published this recall 5 months after the firm started it.

1. Firm started the recall: Aug 28, 202512. FDA classified it Class I: Feb 10, 202623. Published in FDA’s Enforcement Report: Feb 11, 2026320252026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

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

Similar recalls

Latest drug recalls

Keep exploring

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-0304-2026 (August 28, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0304-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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