Aquafaba Powder Vegan Replacement recall
Recalled by 529 Commerce, LLC · Parkland, FL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared Egg
Undeclared allergen: Egg
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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
Quantity: 3860 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
Where it was 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
FDA's distribution note: 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
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern.
- Recalling firm
- 529 Commerce, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 28, 2026
- In FDA report of
- Aug 19, 2026
- FDA recall number
- H-1270-2026 · event 99519
- Official record
- FDA enforcement report search