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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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Low RiskFDA Food
Food & Beverages/Dietary Supplements

TestoFREAK Maximize Testosterone Supplement Recalled for Low Zinc Levels

Agency Publication Date: March 25, 2024
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Summary

VRA FORMULATIONS LLC is recalling approximately 1,569 bottles of TestoFREAK Maximize Testosterone Dietary Supplement because the product contains lower levels of zinc than stated on the label. The supplement is sold in dark amber bottles containing 60 capsules each. No injuries or illnesses have been reported to date, but the product is considered sub-potent. If you purchased this supplement online, you should contact the manufacturer or dispose of the bottle.

Risk

The product contains insufficient levels of zinc, meaning consumers are not receiving the nutritional amount promised on the packaging. This sub-potency may prevent consumers from achieving the intended health benefits of the supplement.

What You Should Do

  1. This recall affects TestoFREAK Maximize Testosterone Dietary Supplement sold in dark amber bottles containing 60 capsules. Check your bottle for lot number 21112002 with an expiration date of 12/2024.
  2. Contact the manufacturer to arrange a return, or throw the product away.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact the manufacturer to arrange return or refund.
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: TestoFREAK Maximize Testosterone Dietary Supplement (60 capsules)
Variants: 60 capsules per bottle
Lot Numbers:
21112002 (Exp 12/2024)

Sold as single bottles or in cases of 100 bottles.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94226
Status: Resolved
Manufacturer: VRA FORMULATIONS LLC
Sold By: internet sales
Manufactured In: United States
Units Affected: 1569 Bottles
Distributed To: Nationwide
Agency Last Updated: April 8, 2024

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.