Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with zipp
Summary
The FDA issued a Class I for Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Reseal by 529 COMMERCE, LLC. Reason: Undeclared Egg.
Details
Source
Food Recall
External ID
H-1270-2026
Action Date
2026-08-19
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
Quantity Affected: 3860 units
Reason for Recall
Undeclared Egg
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
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-28
Company
Parkland, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 63 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (529 COMMERCE, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does 529 COMMERCE, LLC have FDA actions?
This is the only FDA action we have on record for 529 COMMERCE, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1270-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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