FDA recall,
Green Lumber Dietary Supplement
Green Lumber Dietary Supplement may contain undeclared tadalafil, a prescription drug, which can cause life-threatening side effects.
Summary by Recall Canary from the FDA notice
What happened
Green Lumber Holding, LLC issued an updated consumer alert on February 13, 2026, regarding counterfeit products falsely marketed as genuine Green Lumber dietary supplements. The FDA's Enforcement Report referenced the original recall initiated on August 28, 2025, after testing detected tadalafil, an undeclared prescription drug, in products labeled as Green Lumber.
An internal investigation determined a company employee misappropriated packaging and customer information to distribute counterfeit or adulterated products; that employee has been terminated. The counterfeit recalled product bears a specific lot number that is not an authentic Green Lumber lot number. Consumers should not use any product labeled with this lot number, and it should be discarded.
What to do
If a code on your package is listed below:
- What Consumers Should Do Check your packaging: Confirm that your blister packs show one of the following Lot Numbers LOTGL0130151EXP0926; GL01EXP09/27; or GL110725 EXP110727 Immediately discontinue use of any product bearing the Lot number LOT308EXP03/28.
- Report suspected counterfeit product directly to Green Lumber at [phone/email] and to the FDA’s MedWatch Adverse Event Reporting Program.
- Seek medical care promptly if you experience unexpected side effects after using the mislabeled product.
Is yours affected?
Affected if its lot code matches.
counterfeit recalled product
- Lot code
- LOT308EXP03/28
Recall details
- Company announced
- Company
- Green Lumber Holding, LLC.
- Hazard
- Hidden drug ingredient
