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Class I: serious health riskOngoing

529 Commerce Aquafaba Powder Recall

Aquafaba Powder, Vegan Replacement

529 COMMERCE, LLC · Parkland, FL

Risk level
Class I
Reported by FDA
Aug 19, 2026
Recall ID
H-1270-2026
Check your lot numberHow we source this data

Summary

529 Commerce recalled Aquafaba Powder starting Jul 28, 2026. The FDA classified it as Class I (serious health risk) and published enforcement report H-1270-2026 on Aug 19, 2026. Reason: Undeclared Egg. Status: Ongoing.

Why it was recalled

Undeclared Egg

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 numbers, UPCs & expiration codes

Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301

Where it was sold

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 to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-1270-2026
Classification
Class I
Status
Ongoing
Recall initiated
Jul 28, 2026
FDA report date
Aug 19, 2026
Quantity
3860 units
Recall type
Voluntary: Firm initiated
Recalling firm
529 COMMERCE, LLC

Original FDA data

Every field from FDA enforcement report H-1270-2026, exactly as published.

Show all FDA fields
City
Parkland
State
FL
Status
Ongoing
Country
United States
Event ID
99519
Address
6291 Nw 71st Ter
Code information
Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
Postal code
33067-1211
Report date
Aug 19, 2026
Product type
Food
Recall number
H-1270-2026
Classification
Class I
Recalling firm
529 COMMERCE, LLC
Product quantity
3860 units
Reason for recall
Undeclared Egg
Voluntary / mandated
Voluntary: Firm initiated
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
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
Recall initiation date
Jul 28, 2026
Initial firm notification
E-Mail
Center classification date
Aug 26, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-1270-2026, published Aug 19, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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