Recalls and Warnings

Green Lumber Enhancement Supplements Recalled

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If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem.
(Date Posted: 10/26/2019)

On October 22, 2019, GL Holdings issued a recall of Green Lumber, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain tadalafil.

Tadalafil, the active ingredient in Cialis, is prescribed for erectile dysfunction. This drug can cause symptoms like headache and flushing, and can interact with medications containing nitrates such as nitroglycerine, resulting in dangerously low blood pressure.

The lot of Green Lumber capsules that tested positive for tadalafil were distributed between June and August 2019 in the United States and Canada via internet sales. They are sold in 2, 4, and 10-capsule packages with a white wrapper with a green Green Lumber logo on the front. and can be identified by the following:
  • 2 pack: X0020TSV4R
  • 4 pack: X0020TRRHJ
  • 10 Pack: X0020TUJLZ
However, as a precaution, the company is recalling all Green Lumber sold on or before August 10, 2019. Consumers who purchased the recalled capsules should stop consuming them and return any unused product to GL Holdings. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Consumers and healthcare providers can report any adverse reactions to the FDA's MedWatch Voluntary Reporting Program.

(See ConsumerLab.com's Review of Sexual Enhancement Supplements for tests of related products.)

See related warnings:

Liquid Vitamin C for Men Recalled

Titanium 4000 Capsules for Men Recalled

"The Beast" Supplement for Men Recalled

Sexual Enhancement Supplement for Men Recalled

Herbal "Coffee" for Sexual Enhancement Recalled

Herbal "Sexual Enhancement Coffee" Recalled

LEOPARD Miracle Honey Recalled

For more information, use the link below.

GL Holdings Issues Voluntary Worldwide Recall of Green Lumber Products Due to Presence of Undeclared Tadalafil



For other Recalls and Warnings click HERE.
For information about reporting serious reactions and problems with medical products to the U.S. Food and Drug Administration through its MedWatch reporting program, please go to http://www.fda.gov/medwatch/how.htm.


 

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