Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
Alpha Test recall
Recalled by Iovate Health Sciences USA Inc. · Wilmington, DE, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Presence of cathine in product
See the recall's own reason text for the specifics. All other reasons recalls.
What 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
Quantity: Total 163,248 units
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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 it was sold
Arizona California Colorado Connecticut Delaware Florida Georgia Iowa Illinois Indiana Kansas Kentucky Louisiana Michigan Missouri Mississippi North Carolina New Jersey Nevada New York Ohio Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wisconsin
FDA's distribution note: 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
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Iovate Health Sciences USA Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 18, 2024
- In FDA report of
- Feb 5, 2025
- Terminated
- Nov 3, 2025
- FDA recall number
- F-0455-2025 · event 96054
- Official record
- FDA enforcement report search
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