Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10
Recalled by Green Lumber Holdings, LLC
Drug recall
Green Lumber Holdings, LLC
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
Green Lumber Holdings, LLC has recalled Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 11, 2026 and was initiated on August 28, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, with approximately N/A affected. The company behind the recall is Green Lumber Holdings, LLC, based in Corona Del Mar, CA. The FDA describes the product as: “Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660”
Why was Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10 recalled?
According to the FDA, the stated reason for the recall is: “Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil.” In plain terms, this recall relates to an undeclared active substance.
This recall involves an active substance in the product that is not properly declared for how the product is sold. Consuming an active substance without knowing it can be risky, especially for people who take other medications. Clear labeling and approval rules exist to help protect consumers.
What should you do?
If you think you may have bought Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, compare it against the product description and identifying codes (LOT308EXP03/28) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Green Lumber Holdings, LLC or your local health authority.
About this recall
This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- February 11, 2026
- Recall started
- August 28, 2025
- Distributed in
- CA
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10 recalled?+
According to the FDA: Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: D-0304-2026. Information last synced from the FDA on July 6, 2026.