FDA · Class I · August 19, 2026

529 Commerce recall: Aquafaba Powder

529 Commerce, LLC is recalling Aquafaba Powder because of undeclared egg – 3860 units. The U.S. Food and Drug Administration published the recall on August 19, 2026; it began on July 28, 2026. Distributed in 23 states (Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Kansas, Maryland, Massachusetts, Michigan, Minnesota, Nebraska, New York, Oklahoma, Oregon, South Carolina, Tennessee, Texas, Utah, Washington, West Virginia, Wisconsin).

Most serious Class I is the most serious level: a reasonable probability that using or eating the product will cause serious health problems or death.

Produce section of a grocery store
Illustration: Produce section of a grocery store – not the recalled product. Photo: Alabama Extension, CC0, via Wikimedia Commons.
ProductAquafaba Powder
Brand529 Commerce
Company529 Commerce, LLC
TypeFood
ClassificationClass I
Recall dateJuly 28, 2026
Published by FDAAugust 19, 2026
Quantity3860 units
Recall ID99519
As listed by FDA

Recalled 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
    FDA recall number
    H-1270-2026
    Codes, lots and dates
    Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
    Quantity
    3860 units
    Classification
    Class I
Exactly as the agency lists them

Identifiers and details

FDA event ID
99519
Initiated
Voluntary: Firm initiated
Status
Ongoing
Firm location
Parkland, FL, United States

Why it was recalled

The problem: undeclared egg.

The reason the FDA lists: “Undeclared Egg”

Where it was sold

23 states: Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Kansas, Maryland, Massachusetts, Michigan, Minnesota, Nebraska, New York, Oklahoma, Oregon, South Carolina, Tennessee, Texas, Utah, Washington, West Virginia, Wisconsin. Distribution as the FDA records it: “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”

What to do

Check the product name, size, lot code and dates against the list. Do not eat a recalled product, even if it looks and smells fine – throw it away or return it to the store for a refund, and clean surfaces it touched.

Official notice: FDA Enforcement Report record (event 99519, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.

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FAQ

About this recall

Is 529 Commerce Aquafaba Powder recalled?

Yes. 529 Commerce, LLC recalled it on July 28, 2026; FDA published it August 19, 2026 (Class I). Only the lots, dates or models listed on this page are included.

Why was it recalled?

Because of undeclared egg. The reason given: Undeclared Egg

What should I do if I have it?

Check the product name, size, lot code and dates against the list. Do not eat a recalled product, even if it looks and smells fine – throw it away or return it to the store for a refund, and clean surfaces it touched.

Where was it sold?

In 23 states (Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Kansas, Maryland, Massachusetts, Michigan, Minnesota, Nebraska, New York, Oklahoma, Oregon, South Carolina, Tennessee, Texas, Utah, Washington, West Virginia, Wisconsin).

Recalls

More recalls

Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.

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