OVERLOOKED

Recalls › Food

Class IOngoing

529 COMMERCE, LLC recalls Aquafaba Powder

Recall date · record updated Aug 19, 2026 · Source: U.S. Food and Drug Administration (openFDA food enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
529 COMMERCE, LLC
Reason
Undeclared Egg
Hazard
FDA Class I: a reasonable probability that use or exposure will cause serious adverse health consequences or death (FDA definition).
Who’s affected
Distributed to ID, FL, MI, MN, UT, OR, WA, OK, TX, NY, TN, IL, CA, KS, MA, NE, AZ, SC, MD, WI, GA, CO, WA, WV
Where
Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Kansas, Massachusetts, Maryland, Michigan, Minnesota, Nebraska, New York, Oklahoma, Oregon, South Carolina, Tennessee, Texas, Utah, Washington, Wisconsin, West Virginia
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99519…

Products

  1. Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with zipper. UPC 99284 53095 and UPC 99284 30622

    Codes/lots: Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301Quantity: 3860 unitsRecall no. H-1270-2026Class I

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

More Food recalls