US Food Recall Atlas

A single recall record, as the agency published it.

Recall mapAll recalls → F-0455-2025

Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in a cool, dry place (60 F to 80 F), UPC 6-31656-60676-8, SKU0001191, SKU0002075 Iovate Health Sciences USA Inc. · reported 2025-02-05

Terminated This recall has been closed out by the agency.

Reason for recall
Presence of cathine in product
Classification
Class II
Recall initiated
2024-12-18
Reported by the agency
2025-02-05
Closed out (terminated)
2025-11-03
Recalling firm
Iovate Health Sciences USA Inc.
Wilmington, DE
United States

This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.

Distribution (the agency's own words)
Domestic and foreign distribution:NC, CA, TX, NJ, VA, NV, PA, IN, NY, CA, IL,MS, KY, MI,SC, WA, CT, FL, OH, WI, DE, LA, TN, MO, UT, KH, GA, KS, CO, IA, AZ, OR. Foreign distribution: ZA, PH, IS, KZ, AE
States we parsed from that text
AZ CA CO CT DE FL GA IA IL IN KS KY LA MI MO MS NC NJ NV NY OH OR PA SC TN TX UT VA WA WI

The agency named these states. Parse method explicit_state_list, confidence high.

Food category
Dietary supplementsderived

Assigned by a reviewed keyword rulebook over the product description, not by the agency.

Recall type
Voluntary: Firm initiated
Recall number
F-0455-2025

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.