Class IITerminatedVoluntary: Firm initiated
Iovate Health Sciences USA Inc.: food recall F-0455-2025
Iovate Health Sciences USA Inc. of Wilmington, DE recalled Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in… Reason: Presence of cathine in product. The FDA listed it as Class II in its Enforcement Report dated Feb 5, 2025; distribution: Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Missouri, Mississippi, North Carolina, New Jersey, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin.
Record status as published: Terminated (terminated Nov 3, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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
- Product quantity
- Total 163,248 units
- Reason for recall
- Presence of cathine in product
- Codes, lots and dates on the package
- 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)
- 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
- Recalling firm
- Iovate Health Sciences USA Inc., Wilmington, DE
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 18, 2024 |
| Classified by the FDA | Jan 29, 2025 |
| Published in the Enforcement Report | Feb 5, 2025 |
| Terminated | Nov 3, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0455-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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