529 COMMERCE, LLC recalls Aquafaba Powder

529 COMMERCE, LLC started this recall on July 28, 2026. The FDA classified it as Class I, the most serious category: there is a reasonable chance that eating the product could cause serious health problems or death. The reason given is undeclared allergen. It was distributed in 23 states. We consider this recall active, so check your kitchen if you buy this brand.

Status: Active
Recall started: July 28, 2026
Company: 529 COMMERCE, LLC
Classification: Class I (serious health risk)
Where sold: 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
Quantity: 3860 units

Reason for recall (official wording)

Undeclared Egg

Recalled product (official wording)

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

Distribution

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

Compare the brand, size, lot code and dates on your package with the details above. If they match, do not eat it. Throw it away or return it to the store. Contact a healthcare provider if you feel unwell. Step-by-step guide.

Source: FDA Enforcement Report (openFDA), event 99519.