CLASS I ONGOING Food recall · Reported 19 Aug 2026 · FDA Enforcement Report

Aquafaba Powder, Vegan Replacement recalled by 529 Commerce

529 Commerce is recalling Aquafaba Powder, Vegan Replacement, distributed in 23 states. The recall was initiated on 28 Jul 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
Quantity recalled3860 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-1270-2026
FDA event ID
99519
Recalling firm
529 Commerce, Parkland, FL
Classification
Class I
Status
Ongoing
Recall initiated
28 Jul 2026
FDA classified
26 Aug 2026
Reported
19 Aug 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Egg
Product category
Other

Timeline

28 Jul 2026Recall initiated by company
19 Aug 2026Published in enforcement report+22 days
26 Aug 2026Classified by FDA+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared Egg

Product as listed by the FDA

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

Where it was distributed

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

ArizonaCaliforniaColoradoFloridaGeorgiaIdahoIllinoisKansasMassachusettsMarylandMichiganMinnesotaNebraskaNew YorkOklahomaOregonSouth CarolinaTennesseeTexasUtah

Questions about this recall

Is Aquafaba Powder, Vegan Replacement recalled?

Yes. 529 Commerce recalled Aquafaba Powder, Vegan Replacement on 28 Jul 2026. The recall is Class I and its status is Ongoing. Recall number H-1270-2026.

Why was it recalled?

Undeclared Egg

Which lots are affected?

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

Where was it 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 should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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