Food recall

VRA FORMULATIONS LLC recall: TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle

VRA FORMULATIONS LLC, of Medley, FL, recalled TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle. The FDA's reason: “Due to sub-potent levels of Zinc.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on February 6, 2024, and the FDA first listed it in its Enforcement Report of April 3, 2024. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class III

It is unlikely to cause harm

Why

See FDA's words below

Status

Terminated

Closed June 25, 2024

The recall

Company
VRA FORMULATIONS LLC (Medley, FL)
Reason, in FDA's words
“Due to sub-potent levels of Zinc”
Where it was sold
Domestic distribution only through internet sales.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
94226

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-1125-2024 Class III

    TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case

    Codes: Lot Numbers 21112002 Expiration Date: 12/2024

    Quantity: 1569 Bottles

Get new charts weekly

One email a week with the newest charts and their key numbers. No account needed.

Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of April 3, 2024.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.