Recall archive / FDA food enforcement
TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case — FDA record F-1125-2024
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Feb 6, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case
- Reason
- Due to sub-potent levels of Zinc
- Classification
- Class III
- Recalling firm
- VRA FORMULATIONS LLC
- Quantity
- 1569 Bottles
- Agency-reported status
- Terminated
- Source record identifier
- F-1125-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lot Numbers 21112002 Expiration Date: 12/2024 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Domestic distribution only through internet sales.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Apr 3, 2024
- Recall initiation date
- Feb 6, 2024
- Center classification date
- Apr 8, 2024
- Termination date
- Jun 25, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.