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Iovate Health Sciences USA Inc. recall — Alpha Test 120 count Black labeled plastic bottle, 12 bottles per…
FDA (enforcement) · February 5, 2025 · Class II
- Iovate Health Sciences USA Inc. recalled Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count… — an FDA enforcement event posted , classified Class II, covering 1 product entry.
- FDA-stated reason: Presence of cathine in product
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Iovate Health Sciences USA Inc.
- Source ID
- 96054
FDA Enforcement Report search →
Product entries (1)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| F-0455-2025 | 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… | Expiration Date and Lot Codes: March 21, 2027 (Lots 24A125, 24B059, 24B060) March 22,… | Domestic and foreign distribution:NC, CA, TX, NJ, VA, NV,… |
FDA enforcement entries have no per-recall public URL — verify via the FDA Enforcement Report search using the firm name or a recall number above.
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