CLASS I ONGOING Drug recall · Reported 11 Feb 2026 · FDA Enforcement Report

Green Lumber Natural Fuel For Men capsule recalled

Green Lumber Holdings is recalling Green Lumber Natural Fuel For Men capsule, distributed nationwide in the US. The recall was initiated on 28 Aug 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT308EXP03/28
Quantity recalledN/A

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0304-2026
FDA event ID
97526
Recalling firm
Green Lumber Holdings, Corona Del Mar, CA
Classification
Class I
Status
Ongoing
Recall initiated
28 Aug 2025
FDA classified
10 Feb 2026
Reported
11 Feb 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Timeline

28 Aug 2025Recall initiated by company
10 Feb 2026Classified by FDA+166 days
11 Feb 2026Published in enforcement report+1 day

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

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

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

LOT308EXP03/28

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Green Lumber Holdings

All 2
ReportedClassRecallCompanyReasonWhere
DrugCLASS IGreen Lumber Natural Fuel For Men capsule recalledGreen Lumber HoldingsLabeling ErrorsCA