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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

Red Mammoth Male Enhancement Capsules Recalled for Undeclared Drug Ingredients

Agency Publication Date: February 11, 2022
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Summary

Celebrate Today has voluntarily recalled 500 cartons of Red Mammoth male enhancement capsules (400 mg). The capsules were found to contain sildenafil and tadalafil, which are active ingredients in FDA-approved prescription drugs for erectile dysfunction but were not listed on the product label. These products were distributed nationwide throughout the United States via Amazon Marketplace.

Risk

Undeclared sildenafil and tadalafil can interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous or life-threatening levels. Consumers with heart disease, high blood pressure, or diabetes who take nitrates are at significant risk of harm from these unapproved ingredients.

What You Should Do

  1. The recalled products are 400 mg Red Mammoth male enhancement capsules packaged in 10-count blister packs per carton, identified by ASIN B00KA8FBNI and barcode X001ANE0I5.
  2. Check your packaging for lot number DK1027 with an expiration date of 08/01/2023.
  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 Celebrate Today for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 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
๐Ÿ—‘๏ธ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: Red Mammoth capsules (400 mg)
Variants: 10-count blisters
Model:
B00KA8FBNI
X001ANE0I5
Lot Numbers:
DK1027 (Exp. 08/01/2023)

Distributed via Amazon Marketplace.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89563
Status: Resolved
Manufacturer: Celebrate Today
Sold By: Amazon Marketplace
Manufactured In: United States
Units Affected: 500 cartons
Distributed To: Nationwide
Agency Last Updated: February 28, 2022

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 ยท 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.