Class IFood recall: undeclared egg
Aquafaba Powder, Vegan Replacement
529 COMMERCE, LLC, of Parkland, FL, began recalling this product on . FDA classified the recall as Class I on .
Why it was recalled
In FDA’s words:
Undeclared Egg
The allergen tags on this page are ours, matched from FDA’s words above.
The product
Aquafaba Powder, Vegan Replacement
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
- Codes and dates
- Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
- Quantity
- 3860 units
- Recall number
- H-1270-2026
Where it was distributed
In FDA’s words:
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
What Class I means
In FDA’s definitions, a Class I recall is one where: there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. FDA’s recall definitions
If you have this product
- FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
- FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
- If someone has a serious allergic reaction, call 911. Signs of a serious reaction
Source
FDA’s Enforcement Report, read through openFDA. This recall first appeared in the report of . openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.