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RECALL RECORD — CLASS IIIRecall closedF-1125-2024/FDA enforcement
Vra Formulations LLC·Dietary Supplements·Feb 6, 2024

Testofreak Maximize Testosterone Dietary Supplement 60 Capsules Per Dark Amber Bottle, 100…

What you need to know

Class III

  • What happened

    Due to sub-potent levels of Zinc

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDADistribution not listedMore supplements

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Product identification

Source: FDA FOOD

Brand nameVra Formulations LLC
Recalling firmVra Formulations LLCMedley, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot Numbers 21112002 Expiration Date: 12/2024
Distribution area

Domestic distribution only through internet sales.

United States

Quantity affected1569 Bottles
Recall initiationFDA report date: April 3, 2024
FDA recall numberF-1125-2024

Beyond the headline

The recall, in context

Vra Formulations LLC initiated this supplements recall on February 6, 2024. The FDA enforcement report states: Due to sub-potent levels of Zinc. The FDA report lists distribution as: Domestic distribution only through internet sales.

The FDA enforcement report describes the reason as: Due to sub-potent levels of Zinc

Testofreak Maximize Testosterone Dietary Supplement 60 Capsules Per Dark Amber Bottle, 100… was made or distributed by Vra Formulations LLC in Medley, FL, United States. This page reflects FDA report F-1125-2024, dated April 3, 2024.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Testofreak Maximize Testosterone Dietary Supplement 60 Capsules Per Dark Amber Bottle, 100… recall?

Vra Formulations LLC recalled Testofreak Maximize Testosterone Dietary Supplement 60 Capsules Per Dark Amber Bottle, 100… in an FDA Class III enforcement action reported as F-1125-2024. Due to sub-potent levels of Zinc

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Vra Formulations LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1125-2024. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.