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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

Motto International Corp: Sexual Enhancement Capsules Recalled Due to Undeclared Tadalafil

Agency Publication Date: January 10, 2020
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Summary

Motto International Corp is recalling 21 boxes of Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000, and Panther Platinum 30000 capsules because FDA testing found they contain tadalafil. Tadalafil is the active ingredient in Cialis, a prescription drug used for erectile dysfunction, which was not declared on the product labels. These products were sold in Texas in various blister card counts (2, 4, and 10) and feature distinctive hologram or colorful packaging. Consumers should stop using these products and contact their healthcare provider for guidance.

Risk

The undeclared tadalafil in these capsules can interact with nitrates found in some prescription drugs (such as nitroglycerin), potentially lowering blood pressure to dangerous or life-threatening levels. This pose a significant risk to individuals with diabetes, high blood pressure, high cholesterol, or heart disease who often take nitrates.

What You Should Do

  1. Check your medicine cabinet for Bull Platinum 30000 (1000 mg), Stallion Platinum 30000, Rhino 7 Platinum 30000, or Panther Platinum 30000 capsules in 2, 4, or 10-count blister cards.
  2. Verify if your product is affected by checking the packaging: Bull Platinum has an orange/white/yellow background; Stallion Platinum has a blue/orange/white hologram; Rhino 7 has a blue/orange/black hologram; and Panther Platinum has a green/black hologram.
  3. If you have any of these products, stop using them immediately and do not consume any remaining capsules.
  4. Contact your doctor, healthcare provider, or pharmacist if you have experienced any problems that may be related to taking these products.
  5. Return any unused product to the place of purchase for a refund and contact Motto International Corp for further instructions.
  6. For additional questions or to report a side effect, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact healthcare provider and return product for refund.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Bull Platinum 30000 Capsules (1000 mg)
Model:
D-0654-2020
Lot Numbers:
All lots remaining within expiry
Product: Stallion Platinum 30000 Capsules
Model:
D-0655-2020
Lot Numbers:
All lots remaining within expiry
Product: Rhino 7 Platinum 30000 Capsules
Model:
D-0656-2020
Lot Numbers:
All lots remaining within expiry
Product: Panther Platinum 30000 Capsules
Model:
D-0657-2020
Lot Numbers:
All lots remaining within expiry

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84526
Status: Resolved
Manufacturer: Motto International Corp
Manufactured In: United States
Units Affected: 4 products (8 boxes; 7 boxes; 5 boxes; 1 box)
Distributed To: Texas

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.