Green Lumber Holdings Recalls Natural Fuel For Men Capsules
Summary
Green Lumber Holdings, LLC initiated a voluntary Class I recall of its Natural Fuel For Men capsules after FDA analysis found the product contained tadalafil, an unapproved drug ingredient. The recall affects one lot (LOT308EXP03/28) distributed nationwide in 2, 4, 10, and 30-count blister packs. The firm initiated the recall on August 28, 2025; FDA classified it as Class I on February 10, 2026.
What changed
Green Lumber Holdings initiated a voluntary Class I recall of Natural Fuel For Men capsules after FDA analysis determined the product contained tadalafil, an unapproved drug ingredient marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). The affected lot is LOT308EXP03/28, distributed nationwide in various blister pack sizes.\n\nDrug manufacturers and distributors should verify whether they hold or have distributed this product and take appropriate quarantine and removal actions. Consumers who have purchased this product should discontinue use and contact the firm. Class I recalls are the most serious FDA designation, indicating reasonable probability that use of the product will cause adverse health consequences or death.
Archived snapshot
Apr 16, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
Green Lumber Holdings, LLC
Drug Recalls (Class I)
← All Drug Recalls (Class I) Class I D-0304-2026 · 20260211 · Ongoing · Voluntary: Firm initiated
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
Reason for Recall
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
Affected Lot Numbers / Codes
LOT308EXP03/28
Quantity
N/A
Firm Notification Method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Distribution
Nationwide
Initiated
20250828
FDA Classified
20260210
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Source
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