FDA recall, , High risk
Green Lumber Natural Fuel For Men Capsules
Green Lumber Natural Fuel For Men capsule contains undeclared tadalafil, a prescription drug, and may cause life-threatening side effects.
What happened
Green Lumber Holdings, LLC, of Corona Del Mar, California, is voluntarily recalling Green Lumber Natural Fuel For Men capsules after FDA analysis found the product to contain tadalafil, an undeclared prescription drug. The recall, initiated August 28, 2025, was updated on February 13, 2026, to clarify the recalled product lot number. The product was distributed nationwide.
The recalled product is counterfeit and bears a lot number that is not an authentic Green Lumber lot number. Green Lumber's internal investigation determined that a company employee misappropriated legitimate packaging and customer information to distribute counterfeit or adulterated products; that employee has been terminated. Consumers should not use any product labeled with this lot number and should discard it.
What to do
If a code on your package is listed below:
- Do not use any product labeled with this lot number, and it should be discarded.
- Immediately discontinue use of any product bearing the Lot number LOT308EXP03/28.
- Report suspected counterfeit product directly to Green Lumber at [phone/email] and to the FDA’s MedWatch Adverse Event Reporting Program.
- Seek medical care promptly if you experience unexpected side effects after using the mislabeled product.
Is yours affected?
Affected if its lot code matches.
Green Lumber Natural Fuel For Men capsule
- Lot code
- LOT308EXP03/28
Recall details
- Posted by FDA
- Recall began
- Status
- Open
- Weekly archive
- Listed the week of Feb 2, 2026
- Sold in
- Nationwide
- Recalled by
- Green Lumber Holdings, LLCCorona Del Mar, California
- Hazard
- Hidden drug ingredient
- Risk
High risk
There is a reasonable chance that taking it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- FDA event number
- 97526
- Recall number
- D-0304-2026
- Recall type
- Voluntary: Firm initiated
- How the company first told customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
All recalls from Green Lumber Holdings, LLC
Timeline
FDA's Enforcement Report is its public list of recalls; FDA posts a recall by adding it there.
Green Lumber Holdings began the recall
FDA posted the recall to its Enforcement Report
FDA rated the recall Class I (high risk)
Green Lumber Holdings announced the recall
Added to Recall Canary
Summary updated


