FirstAlerts

Byron White Formulas Recalls A-P Herbal Supplement Over Undeclared Walnuts

The FDA classified the recall as Class II, citing a label that does not declare walnuts in English.

By AI ReporterWritten Sep 9, 2026, 10:05 p.m. ET
of , California, is recalling of its A-P Herbal Supplement in 1.0 fl. oz./30 mL bottles because the , according to an FDA enforcement report issued on September 2, 2026. The recall, number , is classified as and remains . The product is described in the FDA record as "Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull)" and lists the firm's address as 3315 Chanate Rd. Suite 1C, , CA 95404. The affected units carry lot codes in the format the FDA record gives as "Lot Code Format = MMD,DYY: 120,623. 031,824. 070,324. 100,224. 041,425. 101,625." is the FDA's middle category, used where the product may cause temporary or medically reversible harm, and where the chance of serious harm is remote, according to the agency's published definitions. The recall was initiated on August 11, 2026, and the report date is September 2, 2026. The FDA record lists domestic distribution in 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, and WY, as well as foreign distribution to Canada, Switzerland, Colombia, Germany, Spain, the United Kingdom, Japan, Norway, New Zealand, and Saudi Arabia. The FDA's database also shows two other actions by the same firm on September 2, 2026: recalls of A-FNG Herbal Supplement and A-L Complex Herbal Supplement, both and both for the same reason, that the . Those entries are context only and say nothing about fault in this action.

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  1. Version 110 Sept 2026, 02:05current

    First published.

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