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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

WEFUN Capsules Recalled for Unapproved Sildenafil Contamination

Agency Publication Date: September 11, 2023
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Summary

Hua Da Trading, Inc. dba Wefun Inc. is recalling 300 cartons of WEFUN Capsules (825 mg). FDA testing discovered that the product is tainted with sildenafil, a prescription-only ingredient found in FDA-approved drugs for male sexual enhancement. Because this medication was marketed without FDA approval, it is considered an unapproved drug. The capsules were sold nationwide in 10-count blister packs through the company's website.

Risk

Sildenafil can interact with nitrates found in some prescription medications, such as nitroglycerin, and may cause a dangerous drop in blood pressure. This pose a serious health risk to individuals with heart disease, high blood pressure, diabetes, or high cholesterol who frequently take nitrate-containing drugs.

What You Should Do

  1. This recall affects WEFUN Capsules (825 mg) sold in 1x10 blister packs per carton, featuring bar code X00358V0O5.
  2. Check your packaging for lot number 18520168 with an expiration date of 09/30/2026.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer at www.eshoponlineusa.com for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for more information regarding this recall.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
🗑️Option 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: WEFUN Capsules (825 mg)
Variants: 825 mg, 1x10 blister pack per carton
Model:
X00358V0O5
Lot Numbers:
18520168 (Exp 09/30/2026)

Manufactured by WEFUN in Brooklyn, NY 11204; available through www.eshoponlineusa.com.

Product Images

Image 1, “WEFUN, Maximize Your Potential, 10 capsules per box”

Image 1, “WEFUN, Maximize Your Potential, 10 capsules per box”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92979
Status: Resolved
Manufacturer: Hua Da Trading, Inc. dba Wefun Inc.
Sold By: www.eshoponlineusa.com
Manufactured In: United States
Units Affected: 300 cartons
Distributed To: Nationwide
Agency Last Updated: September 29, 2023

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release (1) · FDA Press Release (2) · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.