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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

Magnum XXL 9800 Recalled for Undeclared Sildenafil

Agency Publication Date: December 27, 2023
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Summary

Meta Herbal is recalling 500 blister packs of Magnum XXL 9800 (2000 mg per capsule) because it contains sildenafil, an undeclared pharmaceutical ingredient. Sildenafil is the active ingredient in FDA-approved prescription drugs used to treat erectile dysfunction, but it is not authorized for use in this supplement. The product was sold nationwide in the United States through Amazon's Marketplace. If you have used this product, contact your doctor or pharmacist to discuss any health concerns.

Risk

The undeclared sildenafil can interact with nitrates found in some prescription medications, such as nitroglycerin, potentially lowering blood pressure to dangerous levels. This poses a significant risk to individuals with heart disease, high blood pressure, or diabetes who often take nitrate-containing drugs.

What You Should Do

  1. This recall affects Magnum XXL 9800 male sexual enhancement supplements, sold in individual blister packs containing one 2000 mg capsule.
  2. Check your product for UPC 645759993007 and Amazon ASIN numbers B07P7ZH797, B07P94J3ZT, B07P6VK6N3, or B076HNPZZZ. All lots of this product are included in the recall.
  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 for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions.

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: Magnum XXL 9800
Variants: 2000 mg per capsule, 1 capsule per blister pack
UPC Codes:
645759993007
Lot Numbers:
All Lots

Distributed by Magnum Los Angelas CA. Amazon's ASIN# B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ

Product Images

Image 1 - Magnum 9800

Image 1 - Magnum 9800

Image 2 - Magnum 9800 back

Image 2 - Magnum 9800 back

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93510
Status: Active
Manufacturer: Meta Herbal
Sold By: Amazon Marketplace
Manufactured In: United States
Units Affected: 500 blister packs
Distributed To: Nationwide

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.