Class IITerminated in FDA datasetDec 18, 2024

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)

Recalling firm: Iovate Health Sciences USA Inc.

Why it was recalled

Presence of cathine in product

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The exact 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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

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)

TypeCode / valueContext
UPC631656606768 count capsules each per bottle, Store in a cool, dry place (60 F to 80 F), UPC 6-31656-60676-8, SKU0001191, SKU0002075

Recall details

Recall number
F-0455-2025
Event ID
96054
FDA status
Terminated
Initiated
Dec 18, 2024
Reported
Feb 5, 2025
Classified
Jan 29, 2025
Terminated
Nov 3, 2025
Quantity
Total 163,248 units
Location
Wilmington, DE, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

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

FDA source record · F-0455-2025

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.