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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Green Lumber Holdings, LLC: Natural Fuel For Men Recalled for Undeclared Tadalafil

Agency Publication Date: November 15, 2019
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Summary

Green Lumber Holdings, LLC is recalling approximately 30,000 capsules of Green Lumber Natural Fuel For Men because FDA testing found the product contains undeclared Tadalafil. Tadalafil is an FDA-approved drug used to treat erectile dysfunction, but its presence in this herbal supplement makes it an unapproved drug. The affected products were sold in packs of 2, 4, and 10 capsules throughout the United States and Canada via email-based distribution. Consumers should contact their healthcare provider or pharmacist regarding the use of this product and return any remaining capsules to the place of purchase.

Risk

The undeclared Tadalafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates, making this undeclared ingredient a significant health risk.

What You Should Do

  1. Identify if you have Green Lumber Natural Fuel For Men capsules by checking the packaging for the following lot numbers and expiration dates: XC12 (EXP 12/2020), XC06 (EXP 06/2021), XC10 (EXP 10/2021), XC02 (EXP 02/2022), XC04 (EXP 04/2022), or XC06 (EXP 06/2022).
  2. Immediately stop using any affected capsules from the identified lots.
  3. Contact your healthcare provider or pharmacist if you have experienced any problems that may be related to taking this drug product.
  4. Return any unused product to the place of purchase for a refund or contact Green Lumber Holdings, LLC at (949) 426-8622 for further instructions.
  5. For additional questions or to report a related health issue, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Drug product refund and healthcare consultation.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Green Lumber Natural Fuel For Men capsule (2-pack)
Model:
D-0351-2020
Lot Numbers:
XC12 (EXP 12/2020)
XC06 (EXP 06/2021)
XC10 (EXP 10/2021)
XC02 (EXP 02/2022)
XC04 (EXP 04/2022)
XC06 (EXP 06/2022)
Date Ranges: EXP 12/2020, EXP 06/2021, EXP 10/2021, EXP 02/2022, EXP 04/2022, EXP 06/2022
Product: Green Lumber Natural Fuel For Men capsule (4-pack)
Model:
D-0351-2020
Lot Numbers:
XC12 (EXP 12/2020)
XC06 (EXP 06/2021)
XC10 (EXP 10/2021)
XC02 (EXP 02/2022)
XC04 (EXP 04/2022)
XC06 (EXP 06/2022)
Date Ranges: EXP 12/2020, EXP 06/2021, EXP 10/2021, EXP 02/2022, EXP 04/2022, EXP 06/2022
Product: Green Lumber Natural Fuel For Men capsule (10-pack)
Model:
D-0351-2020
Lot Numbers:
XC12 (EXP 12/2020)
XC06 (EXP 06/2021)
XC10 (EXP 10/2021)
XC02 (EXP 02/2022)
XC04 (EXP 04/2022)
XC06 (EXP 06/2022)
Date Ranges: EXP 12/2020, EXP 06/2021, EXP 10/2021, EXP 02/2022, EXP 04/2022, EXP 06/2022

Product Images

GREEN LUMBER, CAPSULE COUNT 2

GREEN LUMBER, CAPSULE COUNT 2

GREEN LUMBER, CAPSULE COUNT 4

GREEN LUMBER, CAPSULE COUNT 4

GREEN LUMBER, CAPSULE COUNT 10

GREEN LUMBER, CAPSULE COUNT 10

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84105
Status: Resolved
Manufacturer: Green Lumber Holdings, LLC
Sold By: Email distribution
Manufactured In: United States
Units Affected: approx. 30,000 capsules
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.