FDA recalls Wefun 825mg capsules due to unapproved drug content containing sildenafil, a substance in FDA-approved male enhancement products. Consumers should stop using and contact the manufacturer.
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil, an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.
The FDA has recalled Wefun 825mg capsules because they contain sildenafil, an ingredient in approved male enhancement drugs, making them unapproved. This poses a risk of serious health effects since the product was marketed without proper FDA approval.
The capsules contain sildenafil, a drug approved for male sexual enhancement, but were marketed without FDA approval. This unapproved drug can cause serious health issues, including cardiovascular problems, as it was not tested for safety.
Anyone who purchased Wefun 825mg capsules from online retailers like eshoponlineusa.com. Men using these capsules for sexual enhancement are at highest risk due to the unapproved sildenafil content.
Check for the brand Wefun, product name 825mg capsules, 1x10 blister pack per carton, manufactured in Brooklyn, NY. The lot number #18520168 and expiration date 09/30/2026 are also on the packaging.
Immediately stop using the recalled Wefun 825mg capsules as they contain unapproved sildenafil, which can cause serious health risks.
The FDA found the capsules contain sildenafil, an ingredient in approved male enhancement drugs, but they were marketed without FDA approval.
Look for the brand Wefun, 825mg capsules, 1x10 blister pack per carton, manufactured in Brooklyn, NY with lot number #18520168 and expiration date 09/30/2026.
Immediately stop using the capsules and contact the manufacturer for further instructions.
We’ve drafted a message you can send Wefun to request your refund or repair — edit it as you like.
Subject: Recall D-1180-2023 — Wefun Wefun Hello, I own a Wefun that is covered by recall D-1180-2023 from Wefun. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
