CLASS II Food recall · Reported 5 Feb 2025 · FDA Enforcement Report
Alpha Test Black labeled recalled by Iovate Health Sciences USA
Iovate Health Sciences USA is recalling Alpha Test Black labeled per, distributed in 30 states. The recall was initiated on 18 Dec 2024 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0455-2025
- FDA event ID
- 96054
- Recalling firm
- Iovate Health Sciences USA, Wilmington, DE
- Brand
- Alpha Test
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 18 Dec 2024
- FDA classified
- 29 Jan 2025
- Reported
- 5 Feb 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Foreign Material
- Product category
- Dietary Supplements
Timeline
| 18 Dec 2024 | Recall initiated by company | |
| 29 Jan 2025 | Classified by FDA | +42 days |
| 5 Feb 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Presence of cathine in product
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
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
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
ArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIowaIllinoisIndianaKansasKentuckyLouisianaMichiganMissouriMississippiNorth CarolinaNew JerseyNevadaNew York
Questions about this recall
Is Alpha Test Black labeled per recalled?
Yes. Iovate Health Sciences USA recalled Alpha Test Black labeled per on 18 Dec 2024. The recall is Class II and its status is Terminated. Recall number F-0455-2025.
Why was it recalled?
Presence of cathine in product
Which lots are affected?
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)
Where was it sold?
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
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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