TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case
Summary
The FDA issued a Class III for TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber b by VRA FORMULATIONS LLC. Reason: Due to sub-potent levels of Zinc.
Details
Source
Food Recall
External ID
F-1125-2024
Action Date
2024-04-03
Status
Terminated
Category
food
Product Description
TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case
Lot/Code Info: Lot Numbers 21112002 Expiration Date: 12/2024
Quantity Affected: 1569 Bottles
Reason for Recall
Due to sub-potent levels of Zinc
Distribution
Domestic distribution only through internet sales.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-06
Company
Medley, FL
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (VRA FORMULATIONS LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does VRA FORMULATIONS LLC have FDA actions?
This is the only FDA action we have on record for VRA FORMULATIONS LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1125-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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