Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules…
Recalling firm: Iovate Health Sciences USA Inc.
Presence of cathine in product
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 3, 2025.
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631656606768FDA 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)
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Full FDA record and distribution details
Original 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
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 631656606768 | count capsules each per bottle, Store in a cool, dry place (60 F to 80 F), UPC 6-31656-60676-8, SKU0001191, SKU0002075 |
Original FDA recall reason
Presence of cathine in product
Recall details
- Recall number
- F-0455-2025
- Event ID
- 96054
- FDA status
- Terminated
- Initiated
- Dec 18, 2024
- Reported
- Feb 5, 2025
- Classified
- Jan 29, 2025
- Terminated
- Nov 3, 2025
- Quantity
- Total 163,248 units
- Location
- Wilmington, DE, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was 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
Data updated September 16, 2026. View official FDA data ↗
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