Green Lumber Holdings, LLC drug recall: Green Lumber Natural Fuel For Men capsule
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Drugs
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 97526
- Recall initiated
- Aug 28, 2025
- Classified by FDA
- Feb 10, 2026
- Posted in Enforcement Report
- Feb 11, 2026
- Recalling firm
- Green Lumber Holdings, LLC
- Firm location
- Corona Del Mar, CA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product, lot or serial numbers below with what you have. If you use a prescription drug or medical device in this recall, talk to your pharmacist or health care provider before you stop using it, and follow the firm's instructions.
Reason for recall
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Aug 28, 2025. FDA classified it 166 days later, on Feb 10, 2026. Distribution reported by FDA: Nationwide Green Lumber Holdings, LLC has 2 recalls in our records.
Recalled products (1)
D-0304-2026 Class I Ongoing
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
Codes / lots: LOT308EXP03/28
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA drug enforcement dataset
- Official notice
- FDA Enforcement Report, event 97526
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.