# FDA recall F-0455-2025

> **Iovate Health Sciences USA Inc.** · Class II · food recall 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

## 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

## Key facts

- **Recall number:** F-0455-2025
- **Recalling firm:** Iovate Health Sciences USA Inc.
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2024-12-18
- **Report date:** 2025-02-05
- **Termination date:** 2025-11-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wilmington, DE, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-0455-2025

## Citation

> AI Analytics. FDA recall F-0455-2025. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/F-0455-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
