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
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
- Brand
- Aquafaba
- 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
- Reason category
- Undeclared Egg
- Product category
- Other
Timeline
| 28 Jul 2026 | Recall initiated by company | |
| 19 Aug 2026 | Published in enforcement report | +22 days |
| 26 Aug 2026 | Classified 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
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 26 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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