Exact FDA event identifier

Event 94226

1 recalled-product record grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: February 06, 2024
Product types: Food
Classifications: Class III
Statuses: Terminated
Recalling firm wording: VRA FORMULATIONS LLC

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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

F-1125-2024

Recall number: F-1125-2024
Initiated: February 06, 2024
Classification: Class III
Status: Terminated
Recalling firm: VRA FORMULATIONS LLC
Quantity: 1569 Bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Due to sub-potent levels of Zinc

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Due to sub-potent levels of Zinc

Code information

Lot Numbers 21112002 Expiration Date: 12/2024

Distribution pattern

Domestic distribution only through internet sales.