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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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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Hi Tech Pharmaceuticals: The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).

Agency Publication Date: June 2, 2021
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Summary

Hi Tech Pharmaceuticals has issued a voluntary recall for Lipodrene With 25mg Ephedra Extract (100-count bottles). The recall affects products sold in 38 states under Lot # 001211197 with an expiration date of 12/25. This action was taken because the FDA found the product contains 1,4-dimethylamylamine (DMAA), an unapproved food additive.

Risk

The product contains 1,4-dimethylamylamine (DMAA), which is considered an unapproved food additive by the FDA and may pose health risks to consumers. While specific incidents were not reported in this notice, the inclusion of unapproved stimulants can cause adverse cardiovascular or neurological effects.

What You Should Do

  1. Check your supplement cabinet for Lipodrene With 25mg Ephedra Extract (100CT) with UPC 8 57084 00056 9.
  2. Verify the lot information on the bottle; specifically look for Lot # 001211197 and an expiration date of 12/25.
  3. If you possess the affected lot, contact Hi Tech Pharmaceuticals or the retail location where it was purchased for instructions on returns or disposal.
  4. Contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional questions.

Affected Products

Product: Lipodrene With 25mg Ephedra Extract (100CT)
UPC Codes:
857084000569
Lot Numbers:
001211197 (Exp. 12/25)
Date Ranges: Exp. 12/25

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87919
Status: Active
Manufacturer: Hi Tech Pharmaceuticals
Manufactured In: United States
Units Affected: 19,068/100 ct bottles

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 · 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.