Lower risk Food recall · FDA · Published August 11, 2026

Byron White Herbal Supplements May Contain Nuts - Label Not in English

Byron White Formulas A-FNG Herbal Supplements (1.0 fl. oz.) may contain nuts but label does not declare walnuts in English. Consumers should check lot codes for affected products.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-1278-2026Food Byron White ›

Lower-risk recall

Label does not declare walnuts in English

✎ GovInfoNow plain-language explainer

Byron White Formulas A-FNG Herbal Supplements (1.:0 fl. oz.) are being recalled because their labels do not declare the presence of walnuts in English. This could pose a risk for people with nut allergies who cannot identify the allergen. Read more at govinfonow.com/recall/686131-byron-white-herbal-supplements-may-contain-nuts-label-not-in.

Source Summary by GovInfoNow · govinfonow.com/recall/686131-byron-white-herbal-supplements-may-contain-nuts-label-not-in · Updated September 14, 2026 · Official notice: FDA #H-1278-2026

Cite this page

“Byron White Herbal Supplements May Contain Nuts - Label Not in English.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/686131-byron-white-herbal-supplements-may-contain-nuts-label-not-in. Based on FDA recall #H-1278-2026.

Byron White Formulas, Inc. voluntarily recalled Byron White FORMULAS A-FNG Herbal Supplement because the label does not declare walnuts in English, posing an allergen risk. The Food and Drug Administration announced the recall on August 11, 2026.

How to tell if you have it

Brand: Byron White
Product: Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull)
Lot Codes: 022,224; 061,424; 092,324; 022,125; 071,825; 112,125; 040,826
Units: 10,403

The hazard

The hazard is that the label does not declare walnuts in English. This undeclared allergen can cause serious or unexpected allergic reactions in sensitive individuals.

Context

GovInfoNow's records show other recent recalls of similar products include Vital Nutrients Aller-C Recall: Undeclared Egg, Soy, Hazelnut (2026-03-27) and Herbs Forever Gastro Care Capsules Recall: Wheat Allergen Risk (2026-01-06). French Broad Chocolate Bake Sale Bonbons Recall: Undeclared Walnut Allergen Risk occurred on 2026-04-23.

How to tell if you have this one

Check the product label for the lot code format MMD,DYY (e.g., 022,224). The product was sold by Byron White Formulas Inc. in Santa Rosa, CA.

Brand
Byron White
Category
Food

FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
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.

Recall number	Product, codes & lots	Quantity
H-1276-2026	Byron White FORMULAS A-L Complex 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; Lot Code Format = MMD,DYY: 012,324. 041,924. 062,824. 092,024. 101,624. 111,324. 071,425. 093,025. 012,026. 042,826.	18,791 units
H-1277-2026	Byron White FORMULAS A-P 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; Lot Code Format = MMD,DYY: 120,623. 031,824. 070,324. 100,224. 041,425. 101,625.	3,486 units
H-1278-2026	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; Lot Code Format = MMD,DYY: 022,224. 061,424. 092,324. 022,125. 071,825. 112,125. 040,826.	10,403 units

Based on the official FDA remedy

What to do — step by step

Check Label for Lot Code
Look for the lot code format MMD,DYY (e.g., 022,224) on the product label.

Where it went and when

Where it was distributed

Distributed in 48 states and D.C. and Puerto Rico, and outside the U.S.

FDA distribution: “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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 22 days after the firm started it.

Aug 11, 2026Firm started the recall
Aug 26, 2026FDA classified it Class II
Sep 2, 2026Published in FDA’s Enforcement Report
Sep 8, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

What should I do if I have the recalled product?

The recall does not require immediate action; check the label for the lot code and contact Byron White Formulas Inc. if you have concerns.

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Link to this recall

<a href="https://govinfonow.com/recall/686131-byron-white-herbal-supplements-may-contain-nuts-label-not-in">Byron White Herbal Supplements May Contain Nuts - Label Not in English (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #H-1278-2026 (August 11, 2026)
Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.