Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494
Summary
The FDA issued a Class I for Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494 by D'Dioses Fruit Pops, Inc.. Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40..
Details
Source
Food Recall
External ID
H-1171-2026
Action Date
2026-07-22
Status
Ongoing
Category
food
Product Description
Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494
Lot/Code Info: 710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225
Quantity Affected: 167 Cases
Reason for Recall
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Distribution
Distributed in the following states: NJ, CT, NY, PA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-04
Company
Paterson, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 39 food recalls issued in the same week, part of 94 food-related FDA actions this month.
D'Dioses Fruit Pops, Inc. has 16 FDA actions in our database, including 16 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (D'Dioses Fruit Pops, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does D'Dioses Fruit Pops, Inc. have FDA actions?
D'Dioses Fruit Pops, Inc. has 16 FDA actions in our database, including 16 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1171-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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