FDA recall record

Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl recall — FDA H-1278-2026

Label does not declare walnuts in English

Class IIclassification
H-1278-2026official record ID
Sep 2, 2026report date

Recall record at a glance

Official recordH-1278-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmByron White Formulas, Inc.
Report dateSep 2, 2026
Recall initiation dateAug 11, 2026
Quantity10,403 units
LocationSanta Rosa, CA, United States

Official product description

Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404

Why the product was recalled

Label does not declare walnuts in English

Distribution information

Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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