Enhancement supplement

Male enhancement supplement recall for undeclared ingredient

A California company has issued a recall for a male sexual enhancement product due to an undeclared ingredient that may interfere with consumers’ prescription drugs.

GL Holdings said the recall impacts Green Lumber dietary supplements, which are packaged in blister packs of 2, 4 and 10 capsules. The company said the products were purchased on or before August 10 and were contaminated with tadalafil, which, when combined with drugs containing nitrates, can cause a drop in blood pressure that can put consumers’ lives in danger.

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It was available for purchase in stores in the United States and Canada, as well as online.

The product is available in packs of 2, 4 and 10 blisters.

“Consumers with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates and may be the population most likely to be affected.” according to the FDA recall notice. “To date, GL Holdings has not received any reports of adverse events related to this recall. “

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The company said it became aware of the problem after an FDA analysis found that much of the product distributed between June and August was contaminated with the ingredient. The FDA has approved tadalafil for the treatment of erectile dysfunction, but not for use in Green Lumber products.

The lots affected by the recall bear the UPC codes: X0020TSV4R, X0020TRRHJ, X0020TUJLZ. Other affected products may be marked on the blister packs with the following: XC12EXP12 / 2020, XC06EXP06 / 2021, XC10EXP10 / 2021, XC02EXP02 / 2022 or XC04EXP04 / 2022.

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Consumers with additional questions are urged to contact GL Holdings by email reminder@greenlumber.com at any time, or by phone at 949-426-8622 Monday through Friday 9:00 a.m. to 5:00 p.m. KST. Peaceful.


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