Iovate Health Sciences USA Inc. recalls Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in…
- Recall date
- December 18, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- F-0455-2025
- FDA classification
- Class II
- Brand / firm
- Iovate Health Sciences USA Inc.
- Sold / 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
Why it was recalled
Presence of cathine in product
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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
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