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Male enhancement supplement recalled over undeclared ingredient

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A California company has made a recall for it to be a male sexual enhancement product and on a declared substance that may affect the consumer’s prescribed medications.

GL as well as the holding companies said the recall, the effects of Green Wood supplements, which have been packaged into 2, 4, and 10-capsule blisters. The company said that the products will be available for purchase on or before Dec. 10), and infected with a dose that, when combined with drugs that contain nitrates, it may result in a decrease in blood pressure, which can be life-threatening for him / her.

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It is 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-capsule blisters.

Consumers with diabetes, high blood pressure, high cholesterol, or heart disease, are often taken as nitrate, and the people most likely to be affected,” according to the FDA recall notice. “To this day, YL Holdings has not received any reports of adverse events related to this recall.”

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The company said it was aware of the problem and, after an FDA analysis found a whole lot of the product was distributed between June and August, it was tainted with the substance. The FDA has approved tadalafil for treatment of erectile dysfunction, but it is not for use on Green Wood products.

The lots affected by the recall bear the UPC code: X0020TSV4R, X0020TRRHJ, X0020TUJLZ. The other products in question to be indicated on the blister packs containing the following: XC12EXP12/2020, XC06EXP06/2021, XC10EXP10/2021, XC02EXP02/2022, or XC04EXP04/2022.

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Consumers with additional questions are urged to get in touch with GL holding corporations, through e-mail recall@greenlumber.com at any time, or by phone at 949-426-8622 Monday through Friday, between the hours of 9 a.m. to 5 p.m. (Pacific Time).

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