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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

Andropharm, LLC: Andropharm Capsules Recalled for Unapproved Anabolic Steroids

Agency Publication Date: September 12, 2017
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Summary

Andropharm, LLC is recalling 1,400 bottles of dietary supplements including ANDROPHARM STEN Z and ANDROPHARM M1 ALPHA because they are marketed without FDA approval and contain anabolic steroids. These products were sold through Andropharm.com, Amazon.com, and in various retail locations in Florida. This recall includes 150 bottles of Sten Z and 1,250 bottles of M1 Alpha, specifically all lots that are currently within their expiration dates.

Risk

The products contain anabolic steroids which are not approved by the FDA; using these substances can lead to serious health issues including liver injury, increased risk of heart attack and stroke, and other hormone-related complications. No specific injuries have been reported in this notice, but the presence of steroids in an unapproved drug poses a critical health risk.

What You Should Do

  1. Check your products for ANDROPHARM STEN Z (60-count bottles) with UPC 6 42125 50294 8 and ANDROPHARM M1 ALPHA (60-count bottles) with UPC 6 42125 50292 4.
  2. Identify if your product is affected by verifying that the lot is still within its expiration date, as all unexpired lots are included in this recall.
  3. Stop using these products immediately and safely dispose of any remaining capsules.
  4. Contact your healthcare provider or pharmacist for guidance regarding any health concerns or potential side effects from using these products.
  5. Return any unused product to the place of purchase for a refund and contact Andropharm, LLC for further instructions regarding this recall.
  6. For additional questions, 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

Drug recall guidance

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

Affected Products

Product: ANDROPHARM STEN Z (60-count bottle)
Model:
Recall #: D-1142-2017
UPC Codes:
642125502948
Lot Numbers:
All lots remaining within expiry
Product: ANDROPHARM M1 ALPHA (60-count bottle)
Model:
Recall #: D-1143-2017
UPC Codes:
642125502924
Lot Numbers:
All lots remaining within expiry

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 77664
Status: Resolved
Manufacturer: Andropharm, LLC
Sold By: Andropharm.com; Amazon.com
Manufactured In: United States
Units Affected: 2 products (150 bottles; 1250 bottles)
Distributed To: Florida

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.