HIGH

Green Lumber Natural Fuel For Men Capsules Recalled for Tadalafil Contamination

Green Lumber Holdings recalled its Natural Fuel For Men capsules on August 28, 2025. The FDA found the capsules contain tadalafil, a prescription ingredient not approved for this product. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Quick Facts at a Glance

Recall Date
August 28, 2025
Hazard Level
HIGH
Brand
Green Lumber Holdings
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Green Lumber Holdings, LLC or your healthcare provider for guidance. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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Product Details

Green Lumber Natural Fuel For Men capsules are packaged in blister packs of 2, 4, 10, and 30-count. The affected model is LOT308EXP03/28. The product distributed nationwide.

The Hazard

The capsules contain tadalafil, which is a prescription drug used for erectile dysfunction. This poses a significant health risk as it can cause serious side effects, especially for individuals with certain medical conditions.

Reported Incidents

No specific incidents, injuries, or deaths have been reported related to this recall. However, the presence of tadalafil in an unapproved product is a serious safety concern.

What to Do

Stop using the capsules immediately. Contact Green Lumber Holdings, LLC or your healthcare provider for further guidance on the recall.

Contact Information

For more information, consumers can visit GreenLumber.com or the FDA recall notice at the provided link.

Key Facts

  • Recalled product: Green Lumber Natural Fuel For Men capsules
  • Contains tadalafil, an unapproved ingredient
  • Recall initiated on August 28, 2025
  • Distributed nationwide
  • Stop using the product immediately

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeDietary Supplement
Sold At
Multiple Retailers

Product Details

Model Numbers
LOT308EXP03/28
Affected States
ALL
Report Date
February 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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