FDAClass I · Food · Recall H-1159-2026 · Recalled July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

Agency report date: July 22, 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: Ice Pop
Company / brand: D'Dioses Fruit Pops
Lot / serial / date codes: 710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225
Distribution: Distributed in the following states: NJ, CT, NY, PA.

Agency product description and boundaries

Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850

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: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

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: Ice Pop

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1159-2026
Brand: D'Dioses Fruit Pops
Classification: Class I
Units affected: 149 Cases
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Ice Pop

Companies & origin

Recalling firm location: Paterson, NJ, United States
Firm address: 287 Marshall St, 07503-3126

Identifying details (verbatim from the notice)

Product codes / lots: 710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225
Distribution: Distributed in the following states: NJ, CT, NY, PA.
Firm notified the public via: Letter
FDA event ID: 99040
Recall initiated: May 4, 2026
FDA classified: July 14, 2026
FDA report date: July 22, 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 September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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