Class IOngoingVoluntary: Firm initiated
529 COMMERCE, LLC: food recall H-1270-2026
529 COMMERCE, LLC of Parkland, FL recalled Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with… Reason: Undeclared Egg. The FDA listed it as Class I in its Enforcement Report dated Aug 19, 2026; distribution: 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.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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
- Product quantity
- 3860 units
- Reason for recall
- Undeclared Egg
- Codes, lots and dates on the package
- Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
- Distribution pattern
- 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
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jul 28, 2026 |
| Classified by the FDA | Aug 26, 2026 |
| Published in the Enforcement Report | Aug 19, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1270-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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