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

Lot, batch or date codesExpiration 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)
Quantity recalledTotal 163,248 units

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
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 2024Recall initiated by company
29 Jan 2025Classified by FDA+42 days
5 Feb 2025Published 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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