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Byron White Formulas, Inc. Recall: Label does not declare walnuts in English

United States

OngoingClass II

Company
Byron White Formulas, Inc.
Product
Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. o…
Recall date
August 11, 2026
Source
FDA

Reason for recall

Label does not declare walnuts in English

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
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 Not published in this source record 18,791 units 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.

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.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-1276-2026
Event ID
99629
Status
Ongoing
Classification
Class II
Company
Byron White Formulas, Inc.
Product description
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
Quantity
18,791 units
Reason
Label does not declare walnuts in English
Recall initiation date
August 11, 2026
Report date
September 2, 2026
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
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.
UPC, lot, and code information
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.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 99629 with 2 other product entries in Public Health Trace.

FDA Recall United States Ongoing 2026 recordClass II

Byron White Formulas, Inc.

Product
Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30…
Published
September 2, 2026
Distribution
Domestic: AK, AL, AR, AZ, CA, CO, CT, DC…

View recall →

FDA Recall United States Ongoing 2026 recordClass II

Byron White Formulas, Inc.

Product
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL…
Published
September 2, 2026
Distribution
Domestic: AK, AL, AR, AZ, CA, CO, CT, DC…

View recall →

Responsible company: Byron White Formulas, Inc.

Other recalls from Byron White Formulas, Inc.

FDA Recall United States Ongoing 2026 recordClass II

Byron White Formulas, Inc.

Product
Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30…
Published
September 2, 2026
Distribution
Domestic: AK, AL, AR, AZ, CA, CO, CT, DC…

View recall →

FDA Recall United States Ongoing 2026 recordClass II

Byron White Formulas, Inc.

Product
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL…
Published
September 2, 2026
Distribution
Domestic: AK, AL, AR, AZ, CA, CO, CT, DC…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Alaska 1
Alabama 1
Arkansas 1
Arizona 1
California 1
Colorado 1
Connecticut 1
District of Columbia 1
Delaware 1
Florida 1
Georgia 1
Hawaii 1
Iowa 1
Idaho 1
Illinois 1
Indiana 1
Kansas 1
Kentucky 1
Louisiana 1
Massachusetts 1
Maryland 1
Maine 1
Michigan 1
Minnesota 1
Missouri 1
Montana 1
North Carolina 1
Nebraska 1
New Hampshire 1
New Jersey 1
New Mexico 1
Nevada 1
New York 1
Ohio 1
Oklahoma 1
Oregon 1
Pennsylvania 1
Puerto Rico 1
Rhode Island 1
South Carolina 1
South Dakota 1
Tennessee 1
Texas 1
Utah 1
Virginia 1
Vermont 1
Washington 1
Wisconsin 1
West Virginia 1
Wyoming 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.