Alpha Test 120 count Black labeled plastic bottle — Class II food recall F-0455-2025
Terminated recall by Iovate Health Sciences USA Inc., reported 2025-02-05, distributed in AZ, CA, CO, CT, DE, FL, GA, IA…. Presence of cathine in product
| Recall number | F-0455-2025 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Iovate Health Sciences USA Inc., Wilmington, DE, United States |
| Recall initiated | 2024-12-18 |
| Classified | 2025-01-29 |
| Reported by FDA | 2025-02-05 |
| Terminated | 2025-11-03 |
| Distributed | 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 |
| Quantity | 163,248 units |
| UPC / GTIN / UDI-DI | 00631656606768 |
| Lot numbers | 24A125, 24B059, 24B060, 24C112, 24E288, 24F164, 24G112, 24G243, 24H207 |
Product
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
Reason for recall
Presence of cathine in product
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0455-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.