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Food FDA Class II Terminated Chemical

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. Published Feb 5, 2025

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 50/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Iovate Health Sciences USA Inc. or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Presence of cathine in product

Hazards

Cathine · primary

Affected products (1)

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

Total 163,248 units

Lot codes: Codes, 24A125, 24C112, 24F164, 24E288, 24G243
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)

Affected areas

ArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIllinoisIndianaIowaKansasKentuckyLouisianaMichiganMississippiMissouriNevadaNew JerseyNew YorkNorth CarolinaOhioOregonPennsylvaniaSouth CarolinaTennesseeTexasUtahVirginiaWashingtonWisconsin

Timeline

  1. Initiated
    Dec 18, 2024
  2. Published
    Feb 5, 2025
  3. Terminated
    Nov 3, 2025
Recall number
F-0455-2025
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.