Byron White FORMULAS A-P Herbal Supplement Recall
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Byron White Formulas, Inc. is recalling 3,486 units of A-P Herbal Supplement because the label does not declare walnuts in English.
FDA recall: what the record actually shows
This notice was issued by FDA on September 8, 2026 and geographically references United States. The FDA classifies this as a Class II recall, with the stated reason "Label does not declare walnuts in English", distributed 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.. FDA recall classes run from I (reasonable probability of serious harm) to III (unlikely to cause harm), so the class number is the fastest way to gauge severity here. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
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What Happened Byron White Formulas, Inc. initiated a voluntary recall of the product because the label does not declare walnuts in English.
Which Products Are Affected Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL. May Contain Nuts (Juglans nigra hull). 3,486 units. Lot Code Format = MMD,DYY: 120,623. 031,824. 070,324. 100,224. 041,425. 101,625. Distributed domestically 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, WY and foreign countries including Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia. Recall number H-1277-2026.
What You Should Do Consumers should verify lot codes on purchased products.
Why This Matters The recall affects 3,486 units distributed across the United States and multiple foreign countries.
Source FDA recall H-1277-2026
Original source: FDA Official Notice ↗
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Elsewhere in the country: similar length or severity timing 8
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