FDA recall record
TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of June 25, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case
Reason
Due to sub-potent levels of Zinc
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case
Code information listed by FDA
Lot Numbers 21112002 Expiration Date: 12/2024
Distribution and firm information
Recalling firm listed by FDA: VRA FORMULATIONS LLC
Firm location listed by FDA: Medley, FL, United States
Distribution reported by FDA: Domestic distribution only through internet sales.
Product quantity listed by FDA: 1569 Bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.