TOPIC: WEFUN Capsules by WEFUN: Recall - Due to Presence of Undeclared Sildenafil
AUDIENCE: Consumer, Health Professional
ISSUE: WEFUN is recalling 300 Boxes of WEFUN Capsules because FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) inhibitor found in FDA-approved products for the treatment of male erectile dysfunction. The presence of sildenafil in this product renders it an unapproved drug for which the safety and efficacy has not been established and, therefore, subject to recall.
Risk Statement: Consumption of products with undeclared sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk.
The affected WEFUN Capsule lot includes the following #18520168 and 09/30/2026. The WEFUN Capsules were distributed Nationwide in the USA via internet sales via amazon.com and eshoponlineusa.com.
WEFUN Inc has not received any reports of adverse events related to this recall.
For more information about this recall, click on the red button "Read Recall" below.
BACKGROUND: The tainted WEFUN Capsules are marketed as a dietary supplement.
RECOMMENDATIONS:
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Consumers/distributors/retailers that have WEFUN Capsules which are being recalled should stop using and return to place of purchase.
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Consumers with questions regarding this recall can contact the company.
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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.
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