FDA Drug Recalls

Recalls / Class I

Class ID-0304-2026

Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.

Product

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

Affected lot / code info
LOT308EXP03/28

Why it was recalled

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

Recalling firm

Firm
Green Lumber Holdings, LLC
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
2855 E Coast Hwy Ste 228, N/A, Corona Del Mar, California 92625-2200

Distribution

Quantity
N/A
Distribution pattern
Nationwide

Timeline

Recall initiated
2025-08-28
FDA classified
2026-02-10
Posted by FDA
2026-02-11
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0304-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.