FDAClass I · Food · Recall H-1137-2026 · Recalled July 8, 2026

a recall — NARA ORGANICS INC

Agency report date: July 8, 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: a
Company / brand: NARA ORGANICS
Lot / serial / date codes: Recalled Lot Codes - 408125075E14F2 - 708125076E14F2 - 708125083E14F2 - 408125139E14F2 - 708125141E14F2 - 708125145E14F2 - 708125174E14F2 - 709125273E14F2 - 709125280E14F2 - 709125288E14F2 - 409125307E14F2 - 70926019ENNB - 70926029ENNB - 70926035ENNB - 70926039ENNB - 70926042ENNB Use-By dates span March 16, 2027 - February 11, 2028
Distribution: nationwide

Agency product description and boundaries

a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 24.7 OZ (700 G); UPC: 860013251901 b.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 14.1 OZ (400 G); UPC: 860013251918

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: Product may be contaminated with Clostridium botulinum.

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: a

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1137-2026
Brand: NARA ORGANICS
Classification: Class I
Units affected: 377,610 cans
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location: New York, NY, United States
Firm address: 250 Greenwich St Fl 39, N/A, 10007-2140

Identifying details (verbatim from the notice)

Product codes / lots: Recalled Lot Codes - 408125075E14F2 - 708125076E14F2 - 708125083E14F2 - 408125139E14F2 - 708125141E14F2 - 708125145E14F2 - 708125174E14F2 - 709125273E14F2 - 709125280E14F2 - 709125288E14F2 - 409125307E14F2 - 70926019ENNB - 70926029ENNB - 70926035ENNB - 70926039ENNB - 70926042ENNB Use-By dates span March 16, 2027 - February 11, 2028
Distribution: nationwide
Firm notified the public via: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID: 99242
Recall initiated: June 13, 2026
FDA classified: July 1, 2026
FDA report date: July 8, 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 ↗

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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 September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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