Class IFood
Aquafaba Powder recall
Summary
529 COMMERCE, LLC is recalling Aquafaba Powder (food). According to the FDA report, the reason is: Undeclared Egg. The FDA rated this a Class I: most serious: there is a reasonable chance the product could cause serious health problems or death. Recall status: Ongoing.
Understanding this recall
What happened
529 Commerce is recalling Aquafaba Powder sold as a vegan egg replacement because it contains egg that isn't declared on the label.
Why it matters
Egg is one of the major food allergens and is especially common in young children. Undeclared egg can cause allergic reactions, including severe ones, in people who rely on labels to avoid it. Aquafaba is often bought specifically to avoid eggs, so undeclared egg here can catch allergic people off guard.
Who should pay attention
People with egg allergies who bought this powder, which was distributed in many states.
Distribution in the FDA report: 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
How to check your product
Check the best-by date and lot number on the foil pouch.
Codes listed by the FDA: Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
Based only on the FDA enforcement record plus general public-health background on this type of hazard. Not medical advice; if you have symptoms or concerns, contact a doctor or pharmacist.
Details from the FDA report
- Product
- 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
- Reason
- Undeclared Egg
- Lot / code info
- Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
- Quantity
- 3860 units
- 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
- Recalling company
- 529 COMMERCE, LLC, Parkland, FL United States
- Recall started
- July 28, 2026
- FDA report date
- August 19, 2026
- Classification
- Class I: Most serious: there is a reasonable chance the product could cause serious health problems or death.
- Voluntary / mandated
- Voluntary: Firm initiated
- Status
- Ongoing
- Recall number
- H-1270-2026
What to do
- Check whether you have this product, and compare the lot numbers, codes, or dates on your package with the codes listed above.
- If it matches, stop using it and keep it away from children and pets.
- Contact the recalling company (529 COMMERCE, LLC) or the store where you bought it about returns or refunds.
- If you think the product made you or someone else sick, contact a doctor or pharmacist. In an emergency call 911.
- You can report problems to the FDA via MedWatch.