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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

Shoreside Enterprises Inc.: POSEIDON Xtreme and 7K Capsules Recalled for Undeclared Drug Ingredients

Agency Publication Date: May 29, 2018
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Summary

Shoreside Enterprises Inc. is recalling POSEIDON Xtreme PLATINUM 4500 (1000mg) and 7K dietary supplement capsules because they contain undeclared sildenafil and tadalafil. These are active ingredients found in FDA-approved prescription drugs for erectile dysfunction; however, their presence in these products makes them unapproved drugs with unestablished safety and efficacy. These supplements were distributed nationwide in single-pack units through various retail channels.

Risk

The undeclared sildenafil and tadalafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and can lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates and are at significant risk of harm.

What You Should Do

  1. Locate any POSEIDON Xtreme PLATINUM 4500 (1000mg) capsules with UPC 638632428857 and Lot 201117BL (Expiration 01/2020).
  2. Locate any 7K capsules with UPC 601577513148 and Lot RO (Expiration 12/31/2021).
  3. Immediately stop using these products and return any unused portions to the place of purchase for a full refund.
  4. Contact your healthcare provider or pharmacist if you have experienced any health problems that may be related to taking these products.
  5. Contact Shoreside Enterprises Inc. at 6345 Newtown Cir Apt A3 Ste A-3, Tampa, Florida, 33615-3629 for further instructions regarding this recall.
  6. For additional questions or to report a complaint, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

Full refund upon return of product.

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

Affected Products

Product: POSEIDON Xtreme PLATINUM 4500 (1000mg)
UPC Codes:
638632428857
Lot Numbers:
201117BL (Exp. 01/2020)
Date Ranges: Expiration 01/2020
Product: 7K capsules
UPC Codes:
601577513148
Lot Numbers:
RO (Exp. 12/31/2021)
Date Ranges: Expiration 12/31/2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 80128
Status: Resolved
Manufacturer: Shoreside Enterprises Inc.
Sold By: Poseidon Distribution Atlanta, GA; SX Power Co. San Diego, CA
Manufactured In: United States
Units Affected: 2 products (Unknown; Unknown)
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 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.