FDAClass I · Food · Recall H-1270-2026 · Recalled August 19, 2026

Aquafaba Powder recall — 529 COMMERCE, LLC

Agency report date: August 19, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Aquafaba Powder
Company / brand: 529 COMMERCE
Lot / serial / date codes: Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
Distribution: 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

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Undeclared Egg

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Aquafaba Powder recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1270-2026
Brand: All 529 COMMERCE recalls
Classification: Class I
Units affected: 3860 units
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Aquafaba Powder recall status

Companies & origin

Recalling firm location: Parkland, FL, United States
Firm address: 6291 Nw 71st Ter, 33067-1211

Identifying details (verbatim from the notice)

Product codes / lots: Best By 12/14/2026 (Lot 1) and Best By 12/12/2027 (Lot 2) Lots: NG2024121501, NG2025121301
Distribution: 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
Firm notified the public via: E-Mail
FDA event ID: 99519
Recall initiated: July 28, 2026
FDA classified: August 26, 2026
FDA report date: August 19, 2026

Other food recalls from around the same time

Organic Whole Blueberries recall — Publix Super Markets, Inc.FDA · August 26, 2026
Organic Whole Blueberries recall — Publix Super Markets, Inc.FDA · August 26, 2026
Cibus Fresh recall — Piazza Produce (dba CIBUS Fresh)FDA · August 19, 2026
TAYLOR FARMS BLEND LETT/ROM BLEND WITH BAG 4/5# Iceberg recall — Taylor Farms de Mexico S. de R.L. de C.V.FDA · August 19, 2026
MARKON BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg recall — Taylor Farms de Mexico S. de R.L. de C.V.FDA · August 19, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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