Recall map → All 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 StatesThis 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
View this record at the agency source →
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.