Byron White Formulas A-L Complex Herbal Supplement Recall
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 18,791 units of A-L Complex Herbal Supplement because the label does not declare walnuts in English.
The full picture behind this FDA recall
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.
A quick skim tells you whether this affects you directly; a closer read tells you more. Check the scope, the source, and how recent the record is, then weigh it against related notices rather than treating any single one as a trend.
The original agency source is linked below so you can verify this record directly before acting on it. Its related labels are recall, product-safety, fda, food.
What Happened
The voluntary recall was initiated because the label does not declare walnuts in English.
Which Products Are Affected
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. 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. Distributed to 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.
What You Should Do
Check lot codes on affected products.
Why This Matters
The recall involves an undeclared allergen in a widely distributed herbal supplement.
Source
FDA recall number H-1276-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Medline Convenience Kits Recall Over ChloraPrep Applicator Sterility Breach (Ref. 2fe0d4)
FDA · September 16, 2026
Cardinal Health Presource Packs Recall Over CliniClean Pericare Wipes Contamination (Ref. 1adab6)
FDA · September 16, 2026
Medline Convenience Kits Recall Over BD ChloraPrep Applicator Seal Issue (Ref. 929d71)
FDA · September 16, 2026
Nationwide notices with 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.
Similar body length
Nearest notices by article body length (1,011 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 8, 2026.
What People Ask
Questions readers often have about this FDA recall.