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ACTIVE RECALL — CLASS IActive recallH-1270-2026/FDA enforcement
529 Commerce, LLC·Food·Jul 28, 2026

Aquafaba Powder, Vegan Replacement, NET WT

What you need to know

Class I

  • What happened

    Undeclared Egg

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Active recall · classified by the FDAID, FL, MI, MN +19 moreMore food

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Product identification

Source: FDA FOOD

Brand name529 Commerce, LLC
Recalling firm529 Commerce, LLCParkland, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
Distribution area
IDFLMIMNUTORWAOKTXNYTNILCAKSMANEAZSCMDWIGACOWV

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

United States

Quantity affected3860 units
Recall initiationFDA report date: August 19, 2026
FDA recall numberH-1270-2026

Beyond the headline

The recall, in context

529 Commerce, LLC initiated this food recall on July 28, 2026. The FDA enforcement report states: Undeclared Egg. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: Undeclared Egg

Aquafaba Powder, Vegan Replacement, NET WT was made or distributed by 529 Commerce, LLC in Parkland, FL, United States. This page reflects FDA report H-1270-2026, dated August 19, 2026.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared egg

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with an egg allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed egg allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have an egg allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Aquafaba Powder, Vegan Replacement, NET WT recall?

529 Commerce, LLC recalled Aquafaba Powder, Vegan Replacement, NET WT in an FDA Class I enforcement action reported as H-1270-2026. Undeclared Egg

What are the symptoms of Undeclared egg exposure?

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with an egg allergy.

How quickly can Undeclared egg symptoms appear?

Reactions can begin within minutes to a few hours after eating the product.

Who is most at risk from Undeclared egg?

People with a diagnosed egg allergy, especially children and anyone with a history of anaphylaxis.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have an egg allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from 529 Commerce, LLC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-1270-2026 and keep the packaging, lot code and proof of purchase if you have them.

Is the 529 Commerce, LLC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-1270-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.