FDA recall H-1270-2026 · Aug 19, 2026
529 COMMERCE, LLC: Aquafaba Powder recall
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 for recall
Undeclared Egg
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- 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
- 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 firm
- 529 COMMERCE, LLC, Parkland, FL
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-28
Source: openFDA enforcement record H-1270-2026 · search recall number H-1270-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
Check something else