Food Recall Check
Class I · High risk Ongoing Initiated May 4, 2026 (5 months ago)

Ice Pop D'Dioses Rompope recall

Recalled by D'Dioses Fruit Pops, Inc. · Paterson, NJ, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

Undeclared allergens: Milk Tree nuts

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Ice Pop, D'Dioses Rompope, 4 oz (85 g), with UPC 710594511812

Quantity: 111 Cases

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225

Where it was sold

Connecticut New Jersey New York Pennsylvania

FDA's distribution note: Distributed in the following states: NJ, CT, NY, PA.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, tree nuts; for anyone else the product is generally not a safety concern.

Recalling firm
D'Dioses Fruit Pops, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 4, 2026
In FDA report of
Jul 22, 2026
FDA recall number
H-1164-2026 · event 99040
Official record
FDA enforcement report search

Also recalled with it (15 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Showing 12 of 15.