Byron White FORMULAS A-P Herbal Supplement Recall

Source: FDA · United States

Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.

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.

It is tempting to skim, check personal relevance, and move on. The better habit is confirming scope, source, and timestamp first, then reading this alongside related notices instead of drawing a conclusion from one record alone.

Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.

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

Beyond this FDA recall's own category, Areazine surfaces two nationwide peer sets: length-matched and severity/date-matched notices from elsewhere in the archive, distinct from the same-feed Related list above.

Common Questions

What people usually ask about a notice like this one.

What is this FDA recall about?
Byron White Formulas, Inc. is recalling 3,486 units of A-P Herbal Supplement because the label does not declare walnuts in English.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How is this recall classified, and why does that matter?
The FDA classifies this as a Class II recall, citing "Label does not declare walnuts in English" as the reason. Class I is the most serious (reasonable probability of serious harm), Class II is a moderate or temporary health risk, and Class III is unlikely to cause harm.
What area is affected?
This alert affects United States. Check with FDA for the most current geographic scope.
Where can I find more FDA Recalls updates?
Browse the full FDA Recalls feed on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.