Class IOngoing · reported 2026-07-22

Ice Pop, D'Dioses Arroz con Leche, 4 oz (85 g), with UPC 710594511843

D'Dioses Fruit Pops, Inc. recalled this product and the FDA reported the enforcement action on 22 July 2026 as Class I. The recall was initiated by the firm. May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product
Ice Pop, D'Dioses Arroz con Leche, 4 oz (85 g), with UPC 710594511843
UPC
710594511843
Reason for recall
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Firm location
Paterson, New Jersey, United States
Classification
Class I
Status
Ongoing
Recall number
H-1160-2026
Quantity
216 Cases
Distribution
Distributed in the following states: NJ, CT, NY, PA.
Initiated
4 May 2026
Reported by FDA
22 July 2026
Firm notified by
Letter
Product codes
710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

  • Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
  • The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
  • This is one of 16 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 16 separate recalls, which almost every published figure does, overstates it by a factor of 16. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 16 of them.
  • This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
  • The distribution pattern names 3 states, and the FDA published the enforcement report 3 months after the firm began the recall.
  • The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

Named in the distribution pattern: Connecticut, New York, Pennsylvania. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.

What this recall was for

Undeclared allergens

An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.

A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.

21 CFR 117.135(c)(2)
Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
21 CFR 101.4
Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
21 CFR 117 subpart G
Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.

The allergens named in this record: milk, tree nuts.

Other records from D'Dioses Fruit Pops, Inc.

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 15 other records name this firm.

ReportedProductFirmReasonClass
2026-07-22Ice Pop, D'Dioses Nuez, 1 Bar (81.7 g), with UPC 827912008548D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Tamarindo, 1 Bar (81.7 g), with UPC 827912008593D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Limon, 4 oz (85 g), with UPC 710594511836D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 710594511362D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Pistachio, 1 Bar (81.7 g), with UPC 827912008487D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Pina Colada, 1 Bar (81.7 g), with UPC 710594511225D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Nanche, 1 Bar (81.7 g), with UPC 827912008449D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Mamey, 1 Bar (81.7 g), with UPC 827912008456D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I

All 16 records for D'Dioses Fruit Pops, Inc.

All 2026 recalls · All FDA food recall data

21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.