Iovate Health Sciences USA Inc.

Recall #F-0455-2025 · Initiated 2024-12-18

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

Quantity affected

Total 163,248 units

Distribution

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

Lot / 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

Initial notification

Letter

Terminated

2025-11-03

Recalling firm

Iovate Health Sciences USA Inc.

1105 N Market St Ste 1330

Wilmington, DE 19801-1241

United States

All recalls from this brand →

Recall classification

Remote probability of serious adverse health consequences, or temporary reversible consequences.