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Lower risk Food recall · FDA · Published July 28, 2026

529 Commerce Aquafaba Powder Recall: Undeclared Egg in Vegan Product

529 Commerce recalls vegan aquafaba powder products due to undeclared egg content. Consumers should check UPCs and best-by dates for affected lots.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-1270-2026Food529 Commerce ›
Official FDA recall photos · click to enlarge
✎ GovInfoNow plain-language explainer

529 Commerce is recalling vegan aquafaba powder products that contain undeclared egg. This poses a risk for people with egg allergies who may experience allergic reactions. Read more at govinfonow.com/recall/686188-529-commerce-aquafaba-powder-recall-undeclared-egg-in-vegan-product.

Source Summary by GovInfoNow · govinfonow.com/recall/686188-529-commerce-aquafaba-powder-recall-undeclared-egg-in-vegan-product · Updated September 14, 2026 · Official notice: FDA #H-1270-2026

Cite this page

“529 Commerce Aquafaba Powder Recall: Undeclared Egg in Vegan Product.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/686188-529-commerce-aquafaba-powder-recall-undeclared-egg-in-vegan-product. Based on FDA recall #H-1270-2026.

The FDA announced on July 28, 2026, that 529 COMMERCE, LLC is recalling Aquafaba Powder due to undeclared egg allergens. Consumers should check their products for specific lot codes and UPCs.

How to tell if you have it

  • Brand: 529 Commerce
  • Product: Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with zipper
  • UPC: 9928453095
  • UPC: 9928430622
  • Best By: 12/14/2026 (Lot NG2024121501)
  • Best By: 12/12/2027 (Lot NG2025121301)

The hazard

The product contains undeclared egg, which poses a risk to individuals with egg allergies. The FDA classified this recall as Class I.

Context

GovInfoNow's records show other recent recalls of similar products include Vital Nutrients Aller-C Recall (2026-03-27) and Jaime's Foods Jalapeno Ranch Recall (2026-08-05). Pearl Milling Pancake Mix Recall occurred on 2026-05-13.

How to tell if you have this one

Check for UPCs 99284 53095 (Best By 12/14/2026, Lot 1) and 99284 30622 (Best By 12/12/2027, Lot 2). The product comes in resealable foil pouches with zipper.

  • Brand
    529 Commerce
  • Product
    Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for UPCs 99284 53095 or 99284 30622 on the packaging to confirm if your product is affected.

Where it went and when

Where it was distributed

Distributed in 23 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: yesIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: not listedMOKentucky: not listedKYWest Virginia: yesWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: yesKSArkansas: not listedARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA 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” States read from FDA’s own wording; “not listed” means the notice does not name it.

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.

Recall timeline

FDA published this recall 22 days after the firm started it.

1. Firm started the recall: Jul 28, 202612. Published in FDA’s Enforcement Report: Aug 19, 202623. FDA classified it Class I: Aug 26, 202634. Added to GovInfoNow: Sep 8, 202642026
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-1270-2026 (July 28, 2026)
  • Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA