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Class II: temporary or reversible health riskTerminated

Iovate Health Sciences Alpha Test 120 count Black labeled plastic Recall

Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count cap…

Iovate Health Sciences USA Inc. · Wilmington, DE

Risk level
Class II
Reported by FDA
Feb 5, 2025
Recall ID
F-0455-2025
Check your lot numberHow we source this data

Summary

Iovate Health Sciences recalled Alpha Test 120 count Black labeled plastic starting Dec 18, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0455-2025 on Feb 5, 2025. Reason: Presence of cathine in product. Status: Terminated.

Why it was recalled

Presence of cathine in product

Product description

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

Lot numbers, UPCs & expiration codes

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)

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0455-2025
Classification
Class II
Status
Terminated
Recall initiated
Dec 18, 2024
FDA report date
Feb 5, 2025
Quantity
Total 163,248 units
Recall type
Voluntary: Firm initiated
Recalling firm
Iovate Health Sciences USA Inc.

Original FDA data

Every field from FDA enforcement report F-0455-2025, exactly as published.

Show all FDA fields
City
Wilmington
State
DE
Status
Terminated
Country
United States
Event ID
96054
Address
1105 N Market St Ste 1330
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)
Postal code
19801-1241
Report date
Feb 5, 2025
Product type
Food
Recall number
F-0455-2025
Classification
Class II
Recalling firm
Iovate Health Sciences USA Inc.
Product quantity
Total 163,248 units
Termination date
Nov 3, 2025
Reason for recall
Presence of cathine in product
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
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
Recall initiation date
Dec 18, 2024
Initial firm notification
Letter
Center classification date
Jan 29, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0455-2025, published Feb 5, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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