Green Lumber Natural Fuel For Men capsule, packaged in packs of 2, 4 and 10 capsules, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660 (949) 426-8622.

Recall Insight

This FDA Drug action (record #D-0351-2020) was formally reported on November 13, 2019, with the manufacturer initiating the action on October 22, 2019. It is classified under Critical severity (Class I), with a current status of Terminated. Green Lumber Holdings, LLC is listed as the recalling firm, operating out of Corona Del Mar, CA. Federal records indicate approx. 30,000 capsules units are affected.

The documented reason for this recall is: Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain undeclared Tadalafil, an FDA approved drug for the treatment of erectile dysfunction. Distribution data in the federal record shows the product reached: United States and Canada. Only email addresses were provided, no physical address information was received.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 5 were also issued by FDA Drug. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 7 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.