Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported February 5, 2025
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
Presence of cathine in product
Iovate Health Sciences USA Inc. recalled Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsu… - a moderate-severity action.
Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsu… was recalled by Iovate Health Sciences USA Inc. in February 5, 2025. Reason: Presence of cathine in product. Check the official notice for the remedy. Verify recall #F-0455-2025 with the FDA Food before acting.
The recall
Iovate Health Sciences USA Inc. issued this moderate-severity FDA Food recall-Presence of cathine in product.
- Moderate
- severity level
- Class II
- classification
- February 5, 2025
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0455-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0455-2025) was formally reported on February 5, 2025, with the manufacturer initiating the action on December 18, 2024. It is classified under Moderate severity (Class II), with a current status of Terminated. Iovate Health Sciences USA Inc. is listed as the recalling firm, operating out of Wilmington, DE. Federal records list the affected scope as Total 163,248 units.
The documented reason for this recall is: Presence of cathine in product Distribution data in the federal record shows the product reached: 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. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
Total 163,248 units
Related Recalls
6
0 from same agency
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
Reason for recall
Presence of cathine in product
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0455-2025 |
| Date reported | February 5, 2025 |
| Date initiated | December 18, 2024 |
| Recalling firm | Iovate Health Sciences USA Inc. |
| Firm location | Wilmington, DE |
| Affected scope | Total 163,248 units |
| 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 |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0455-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product 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. Recalled by Iovate Health Sciences USA Inc.. Units affected: Total 163,248 units.
Why was this product recalled? ▼
Presence of cathine in product
Which agency issued this recall? ▼
This recall was issued by the FDA Food on February 5, 2025. Severity: Moderate. Recall number: F-0455-2025.
Where was the recalled product distributed? ▼
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.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0455-2025) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported February 5, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.