MODERATE RISK
Terminated
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
Recalled by Iovate Health Sciences USA Inc.
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
Reason for Recall
Presence of cathine in product
Product Details
Product Quantity
Total 163,248 units
Product Type
Food
Code Info
Expiration Date and Lot Codes: March 21, 2027 (Lots 24A125, 24B059, 24B060) March 22, 2027 (Lot 24C112) July 3, 2027 (Lots 24F164, 24G112) July 4, 2027 (Lot 24E288) July 5, 2027 (Lots 24G243, 24H207)
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
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
Company Location
Wilmington, DE, 19801-1241
Timeline
Report Date
02/05/2025
Recall Initiated
12/18/2024
Classification Date
01/29/2025
Termination Date
11/03/2025
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 28, 2026
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